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Unexplained young onset end-stage renal disease v4.7 Achchuthan Shanmugasundram Changed child panels to: Cystic kidney disease; Renal tubulopathies; Proteinuric renal disease; Nephrocalcinosis or nephrolithiasis; Renal ciliopathies; Atypical haemolytic uraemic syndrome; Tubulointerstitial kidney disease; Membranoproliferative glomerulonephritis including C3 glomerulopathy; Haematuria; Hereditary systemic amyloidosis; Unexplained young onset end-stage renal disease - additional genes
Panel types changed to GMS Rare Disease Virtual; Super Panel; GMS Rare Disease; GMS signed-off
Unexplained young onset end-stage renal disease - additional genes v0.2 ISCA-37401-Loss Achchuthan Shanmugasundram commented on Region: ISCA-37401-Loss
Unexplained young onset end-stage renal disease - additional genes v0.2 WDR72 Achchuthan Shanmugasundram commented on gene: WDR72
Unexplained young onset end-stage renal disease - additional genes v0.2 FAN1 Achchuthan Shanmugasundram commented on gene: FAN1
Unexplained young onset end-stage renal disease - additional genes v0.2 UPK3A Achchuthan Shanmugasundram commented on gene: UPK3A
Unexplained young onset end-stage renal disease - additional genes v0.2 UPK2 Achchuthan Shanmugasundram commented on gene: UPK2
Unexplained young onset end-stage renal disease - additional genes v0.2 TSHZ3 Achchuthan Shanmugasundram commented on gene: TSHZ3
Unexplained young onset end-stage renal disease - additional genes v0.2 TNXB Achchuthan Shanmugasundram commented on gene: TNXB
Unexplained young onset end-stage renal disease - additional genes v0.2 SPRY1 Achchuthan Shanmugasundram commented on gene: SPRY1
Unexplained young onset end-stage renal disease - additional genes v0.2 SOX17 Achchuthan Shanmugasundram commented on gene: SOX17
Unexplained young onset end-stage renal disease - additional genes v0.2 SMARCA4 Achchuthan Shanmugasundram commented on gene: SMARCA4
Unexplained young onset end-stage renal disease - additional genes v0.2 SLIT2 Achchuthan Shanmugasundram commented on gene: SLIT2
Unexplained young onset end-stage renal disease - additional genes v0.2 SIX1 Achchuthan Shanmugasundram commented on gene: SIX1
Unexplained young onset end-stage renal disease - additional genes v0.2 SHH Achchuthan Shanmugasundram commented on gene: SHH
Unexplained young onset end-stage renal disease - additional genes v0.2 ROBO2 Achchuthan Shanmugasundram commented on gene: ROBO2
Unexplained young onset end-stage renal disease - additional genes v0.2 MYH11 Achchuthan Shanmugasundram commented on gene: MYH11
Unexplained young onset end-stage renal disease - additional genes v0.2 KIT Achchuthan Shanmugasundram commented on gene: KIT
Unexplained young onset end-stage renal disease - additional genes v0.2 HCN3 Achchuthan Shanmugasundram commented on gene: HCN3
Unexplained young onset end-stage renal disease - additional genes v0.2 GREM1 Achchuthan Shanmugasundram commented on gene: GREM1
Unexplained young onset end-stage renal disease - additional genes v0.2 GDNF Achchuthan Shanmugasundram commented on gene: GDNF
Unexplained young onset end-stage renal disease - additional genes v0.2 FOXC2 Achchuthan Shanmugasundram commented on gene: FOXC2
Unexplained young onset end-stage renal disease - additional genes v0.2 FOXC1 Achchuthan Shanmugasundram commented on gene: FOXC1
Unexplained young onset end-stage renal disease - additional genes v0.2 DLG3 Achchuthan Shanmugasundram commented on gene: DLG3
Unexplained young onset end-stage renal disease - additional genes v0.2 DACT1 Achchuthan Shanmugasundram commented on gene: DACT1
Unexplained young onset end-stage renal disease - additional genes v0.2 COX10 Achchuthan Shanmugasundram commented on gene: COX10
Unexplained young onset end-stage renal disease - additional genes v0.2 CHD1L Achchuthan Shanmugasundram commented on gene: CHD1L
Unexplained young onset end-stage renal disease - additional genes v0.2 BMP4 Achchuthan Shanmugasundram commented on gene: BMP4
Unexplained young onset end-stage renal disease - additional genes v0.2 BICC1 Achchuthan Shanmugasundram commented on gene: BICC1
Unexplained young onset end-stage renal disease - additional genes v0.2 ACTA2 Achchuthan Shanmugasundram commented on gene: ACTA2
Unexplained young onset end-stage renal disease - additional genes v0.2 BNC2 Achchuthan Shanmugasundram commented on gene: BNC2
Unexplained young onset end-stage renal disease - additional genes v0.2 RET Achchuthan Shanmugasundram commented on gene: RET
Unexplained young onset end-stage renal disease - additional genes v0.2 CHRM3 Achchuthan Shanmugasundram commented on gene: CHRM3
Unexplained young onset end-stage renal disease - additional genes v0.2 ARMC9 Achchuthan Shanmugasundram commented on gene: ARMC9
Unexplained young onset end-stage renal disease - additional genes v0.2 RMND1 Achchuthan Shanmugasundram commented on gene: RMND1
Unexplained young onset end-stage renal disease - additional genes v0.2 TRAP1 Achchuthan Shanmugasundram commented on gene: TRAP1
Unexplained young onset end-stage renal disease - additional genes v0.2 TBX18 Achchuthan Shanmugasundram commented on gene: TBX18
Unexplained young onset end-stage renal disease - additional genes v0.2 SIX5 Achchuthan Shanmugasundram commented on gene: SIX5
Unexplained young onset end-stage renal disease - additional genes v0.2 SALL1 Achchuthan Shanmugasundram commented on gene: SALL1
Unexplained young onset end-stage renal disease - additional genes v0.2 RRM2B Achchuthan Shanmugasundram commented on gene: RRM2B
Unexplained young onset end-stage renal disease - additional genes v0.2 PBX1 Achchuthan Shanmugasundram commented on gene: PBX1
Unexplained young onset end-stage renal disease - additional genes v0.2 LRIG2 Achchuthan Shanmugasundram commented on gene: LRIG2
Unexplained young onset end-stage renal disease - additional genes v0.2 KYNU Achchuthan Shanmugasundram commented on gene: KYNU
Unexplained young onset end-stage renal disease - additional genes v0.2 ITGA8 Achchuthan Shanmugasundram commented on gene: ITGA8
Unexplained young onset end-stage renal disease - additional genes v0.2 HPSE2 Achchuthan Shanmugasundram commented on gene: HPSE2
Unexplained young onset end-stage renal disease - additional genes v0.2 HAAO Achchuthan Shanmugasundram commented on gene: HAAO
Unexplained young onset end-stage renal disease - additional genes v0.2 GRIP1 Achchuthan Shanmugasundram commented on gene: GRIP1
Unexplained young onset end-stage renal disease - additional genes v0.2 GLI3 Achchuthan Shanmugasundram commented on gene: GLI3
Unexplained young onset end-stage renal disease - additional genes v0.2 GATA3 Achchuthan Shanmugasundram commented on gene: GATA3
Unexplained young onset end-stage renal disease - additional genes v0.2 FREM2 Achchuthan Shanmugasundram commented on gene: FREM2
Unexplained young onset end-stage renal disease - additional genes v0.2 FREM1 Achchuthan Shanmugasundram commented on gene: FREM1
Unexplained young onset end-stage renal disease - additional genes v0.2 FRAS1 Achchuthan Shanmugasundram commented on gene: FRAS1
Unexplained young onset end-stage renal disease - additional genes v0.2 EYA1 Achchuthan Shanmugasundram commented on gene: EYA1
Unexplained young onset end-stage renal disease - additional genes v0.2 DSTYK Achchuthan Shanmugasundram commented on gene: DSTYK
Unexplained young onset end-stage renal disease - additional genes v0.2 CHD7 Achchuthan Shanmugasundram commented on gene: CHD7
Unexplained young onset end-stage renal disease - additional genes v0.2 ANOS1 Achchuthan Shanmugasundram commented on gene: ANOS1
Unexplained young onset end-stage renal disease - additional genes v0.2 AGTR1 Achchuthan Shanmugasundram commented on gene: AGTR1
Unexplained young onset end-stage renal disease - additional genes v0.2 AGT Achchuthan Shanmugasundram commented on gene: AGT
Unexplained young onset end-stage renal disease - additional genes v0.2 ACTG2 Achchuthan Shanmugasundram commented on gene: ACTG2
Unexplained young onset end-stage renal disease - additional genes v0.2 ACE Achchuthan Shanmugasundram commented on gene: ACE
Unexplained young onset end-stage renal disease - additional genes v0.1 ISCA-37401-Loss Achchuthan Shanmugasundram Region: ISCA-37401-Loss was added
Region: ISCA-37401-Loss was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for Region: ISCA-37401-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for Region: ISCA-37401-Loss were set to 194072; Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
Unexplained young onset end-stage renal disease - additional genes v0.1 WDR72 Achchuthan Shanmugasundram gene: WDR72 was added
gene: WDR72 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,NHS GMS,Expert Review
Mode of inheritance for gene: WDR72 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: WDR72 were set to 31959358; 30779877; 30028003; 33033857
Phenotypes for gene: WDR72 were set to Amelogenesis imperfecta, type IIA3, OMIM:613211; hereditary distal renal tubular acidosis; amelogenesis imperfecta hypomaturation type 2A3, MONDO:0013181; distal renal tubular acidosis, MONDO:0015827
Unexplained young onset end-stage renal disease - additional genes v0.1 UPK3A Achchuthan Shanmugasundram gene: UPK3A was added
gene: UPK3A was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: UPK3A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: UPK3A were set to Renal Adysplasia
Unexplained young onset end-stage renal disease - additional genes v0.1 UPK2 Achchuthan Shanmugasundram gene: UPK2 was added
gene: UPK2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: UPK2 was set to Other
Unexplained young onset end-stage renal disease - additional genes v0.1 TSHZ3 Achchuthan Shanmugasundram gene: TSHZ3 was added
gene: TSHZ3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: TSHZ3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 TRAP1 Achchuthan Shanmugasundram gene: TRAP1 was added
gene: TRAP1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: TRAP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TRAP1 were set to 24152966
Phenotypes for gene: TRAP1 were set to CAKUT; VACTERL 192350
Unexplained young onset end-stage renal disease - additional genes v0.1 TNXB Achchuthan Shanmugasundram gene: TNXB was added
gene: TNXB was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: TNXB was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 TBX18 Achchuthan Shanmugasundram gene: TBX18 was added
gene: TBX18 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: TBX18 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: TBX18 were set to Congenital anomalies of kidney and urinary tract 2 143400
Unexplained young onset end-stage renal disease - additional genes v0.1 SPRY1 Achchuthan Shanmugasundram gene: SPRY1 was added
gene: SPRY1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SPRY1 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 SOX17 Achchuthan Shanmugasundram gene: SOX17 was added
gene: SOX17 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SOX17 was set to Unknown
Phenotypes for gene: SOX17 were set to Vesicoureteral reflux 3, 613674
Unexplained young onset end-stage renal disease - additional genes v0.1 SMARCA4 Achchuthan Shanmugasundram gene: SMARCA4 was added
gene: SMARCA4 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SMARCA4 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 SLIT2 Achchuthan Shanmugasundram gene: SLIT2 was added
gene: SLIT2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SLIT2 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 SIX5 Achchuthan Shanmugasundram gene: SIX5 was added
gene: SIX5 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: SIX5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SIX5 were set to Branchiootorenal syndrome 2, 610896
Unexplained young onset end-stage renal disease - additional genes v0.1 SIX1 Achchuthan Shanmugasundram gene: SIX1 was added
gene: SIX1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SIX1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: SIX1 were set to Branchiootorenal Spectrum Disorders
Unexplained young onset end-stage renal disease - additional genes v0.1 SHH Achchuthan Shanmugasundram gene: SHH was added
gene: SHH was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: SHH was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 SALL1 Achchuthan Shanmugasundram gene: SALL1 was added
gene: SALL1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: SALL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SALL1 were set to Townes-Brocks syndrome, 107480; Townes-Brocks branchiootorenal-like syndrome, 107480; imperforate anus, ear abnormalities, thumb abnormalities
Unexplained young onset end-stage renal disease - additional genes v0.1 RRM2B Achchuthan Shanmugasundram gene: RRM2B was added
gene: RRM2B was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: RRM2B was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: RRM2B were set to Mitochondrial DNA depletion syndrome 8A (encephalomyopathic,renal tubulopathy), 612075; Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy) 612075; Mitochondrial DNA depletion syndrome 8B (MNGIE type) 612075
Unexplained young onset end-stage renal disease - additional genes v0.1 ROBO2 Achchuthan Shanmugasundram gene: ROBO2 was added
gene: ROBO2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: ROBO2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: ROBO2 were set to Vesicoureteral Reflux; Vesicoureteral reflux 2, 610878
Unexplained young onset end-stage renal disease - additional genes v0.1 RMND1 Achchuthan Shanmugasundram gene: RMND1 was added
gene: RMND1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,NHS GMS,Literature
Mode of inheritance for gene: RMND1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RMND1 were set to 31568715; 31889854; 32911714
Phenotypes for gene: RMND1 were set to Combined oxidative phosphorylation deficiency 11, OMIM:614922
Unexplained young onset end-stage renal disease - additional genes v0.1 RET Achchuthan Shanmugasundram gene: RET was added
gene: RET was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: RET was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: RET were set to Multiple endocrine neoplasia IIA, 171400; Renal agenesis, 191830; Renal Adysplasia; Pheochromocytoma, 171300; Medullary thyroid carcinoma, 155240; {Hirschsprung disease, susceptibility to, 1}, 142623; Multiple endocrine neoplasia IIB, 162300; Central hypoventilation syndrome, congenital, 209880
Unexplained young onset end-stage renal disease - additional genes v0.1 PBX1 Achchuthan Shanmugasundram gene: PBX1 was added
gene: PBX1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: PBX1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: PBX1 were set to 28270404; 28566479
Phenotypes for gene: PBX1 were set to CAKUT
Unexplained young onset end-stage renal disease - additional genes v0.1 MYH11 Achchuthan Shanmugasundram gene: MYH11 was added
gene: MYH11 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: MYH11 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYH11 were set to Megacystis-microcolon-intestinal hypoperistalsis syndrome
Unexplained young onset end-stage renal disease - additional genes v0.1 LRIG2 Achchuthan Shanmugasundram gene: LRIG2 was added
gene: LRIG2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: LRIG2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LRIG2 were set to Stuart HM, Roberts NA, Bergu B, Daly SB, Urquhart JE, Bhaskar S, Dickerson J, Mermerkaya M, Silay MS, Lewis MA, Olondriz BO, Gener B, Beetz C, Varga RE, G lp nar O, S er E, Yal nkaya F, G c k A, Yue WW, Erdogan F, Berry A, Hanley NA, McKenzie EA, Hilton EN, Woolf AS, Newman WG. LRIG2 mutations cause urofacial syndrome. Am J Hum Genet 92:259-264, 2013.
Phenotypes for gene: LRIG2 were set to Urofacial syndrome 2 615112; Urofacial syndrome; Congenital bladder disease: dyssynergic, high pressure bladder.
Unexplained young onset end-stage renal disease - additional genes v0.1 KYNU Achchuthan Shanmugasundram gene: KYNU was added
gene: KYNU was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: KYNU was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: KYNU were set to 28792876; 27604308; 17334708
Phenotypes for gene: KYNU were set to Hydroxykynureninuria (Disorders of histidine, tryptophan or lysine metabolism); VACTERL-like phenotype; multiple congenital malformations; ?Hydroxykynureninuria, 236800
Unexplained young onset end-stage renal disease - additional genes v0.1 KIT Achchuthan Shanmugasundram gene: KIT was added
gene: KIT was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: KIT was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 ITGA8 Achchuthan Shanmugasundram gene: ITGA8 was added
gene: ITGA8 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: ITGA8 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ITGA8 were set to Renal hypodysplasia/aplasia 1, 191830
Unexplained young onset end-stage renal disease - additional genes v0.1 HPSE2 Achchuthan Shanmugasundram gene: HPSE2 was added
gene: HPSE2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: HPSE2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HPSE2 were set to 20560209; 20560210
Phenotypes for gene: HPSE2 were set to Congenital bladder disease: dyssynergic, high pressure bladder; Urofacial syndrome 1 236730; Urofacial Syndrome
Unexplained young onset end-stage renal disease - additional genes v0.1 HCN3 Achchuthan Shanmugasundram gene: HCN3 was added
gene: HCN3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: HCN3 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 HAAO Achchuthan Shanmugasundram gene: HAAO was added
gene: HAAO was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: HAAO was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HAAO were set to 28792876; 27604308; 17334708
Phenotypes for gene: HAAO were set to Multiple congenital malformations; VACTERL-like phenotype
Unexplained young onset end-stage renal disease - additional genes v0.1 GRIP1 Achchuthan Shanmugasundram gene: GRIP1 was added
gene: GRIP1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: GRIP1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GRIP1 were set to 24700879; 22510445; 14730302; 24357607
Phenotypes for gene: GRIP1 were set to isolated CAKUT; Fraser syndrome; Fraser syndrome 219000
Unexplained young onset end-stage renal disease - additional genes v0.1 GREM1 Achchuthan Shanmugasundram gene: GREM1 was added
gene: GREM1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: GREM1 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 GLI3 Achchuthan Shanmugasundram gene: GLI3 was added
gene: GLI3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: GLI3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: GLI3 were set to Pallister-Hall syndrome, OMIM:146510
Unexplained young onset end-stage renal disease - additional genes v0.1 GDNF Achchuthan Shanmugasundram gene: GDNF was added
gene: GDNF was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: GDNF was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 GATA3 Achchuthan Shanmugasundram gene: GATA3 was added
gene: GATA3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: GATA3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: GATA3 were set to Hypoparathyroidism, sensorineural deafness, and renal dysplasia, 146255; Hypoparathyroidism, Sensorineural Deafness, and Renal Disease
Unexplained young onset end-stage renal disease - additional genes v0.1 FREM2 Achchuthan Shanmugasundram gene: FREM2 was added
gene: FREM2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: FREM2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FREM2 were set to Fraser syndrome; Fraser syndrome 219000
Unexplained young onset end-stage renal disease - additional genes v0.1 FREM1 Achchuthan Shanmugasundram gene: FREM1 was added
gene: FREM1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: FREM1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FREM1 were set to PMID: 24700879
Phenotypes for gene: FREM1 were set to Bifid nose with or without anorectal and renal anomalies, 608980
Unexplained young onset end-stage renal disease - additional genes v0.1 FRAS1 Achchuthan Shanmugasundram gene: FRAS1 was added
gene: FRAS1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: FRAS1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FRAS1 were set to Fraser syndrome; Fraser syndrome 219000
Unexplained young onset end-stage renal disease - additional genes v0.1 FOXC2 Achchuthan Shanmugasundram gene: FOXC2 was added
gene: FOXC2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: FOXC2 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 FOXC1 Achchuthan Shanmugasundram gene: FOXC1 was added
gene: FOXC1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: FOXC1 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 FAN1 Achchuthan Shanmugasundram gene: FAN1 was added
gene: FAN1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,Expert Review
Mode of inheritance for gene: FAN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FAN1 were set to 35931300; 22772369
Phenotypes for gene: FAN1 were set to karyomegalic interstitial nephritis, MONDO:0013898; Interstitial nephritis, karyomegalic, OMIM:614817; interstitial nephritis; chronic kidney disease
Unexplained young onset end-stage renal disease - additional genes v0.1 EYA1 Achchuthan Shanmugasundram gene: EYA1 was added
gene: EYA1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: EYA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: EYA1 were set to Branchiootic syndrome 1, 602588; Branchiootorenal syndrome 1, with or without cataracts, 113650; Anterior segment anomalies with or without cataract, 113650; Branchiootorenal syndrome 1, with or without cataracts; Otofaciocervical syndrome, 166780; Branchiootorenal Spectrum Disorders
Unexplained young onset end-stage renal disease - additional genes v0.1 DSTYK Achchuthan Shanmugasundram gene: DSTYK was added
gene: DSTYK was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: DSTYK was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: DSTYK were set to ureteropelvic junction obstruction; CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1; Renal hypodysplasia; {Congenital anomalies of kidney and urinary tract, susceptibility to}; vesicoureteric reflux; {Congenital anomalies of kidney and urinary tract, susceptibility to}, 610805
Unexplained young onset end-stage renal disease - additional genes v0.1 DLG3 Achchuthan Shanmugasundram gene: DLG3 was added
gene: DLG3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: DLG3 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 DACT1 Achchuthan Shanmugasundram gene: DACT1 was added
gene: DACT1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: DACT1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: DACT1 were set to 22610794; 19701191; 28054444
Phenotypes for gene: DACT1 were set to ?Townes-Brocks syndrome 2,617466; TBS2
Unexplained young onset end-stage renal disease - additional genes v0.1 COX10 Achchuthan Shanmugasundram gene: COX10 was added
gene: COX10 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: COX10 was set to Unknown
Phenotypes for gene: COX10 were set to Encephalopathy, progressive mitochondrial, with proximal renal tubulopathy due tocytochrome c oxidase deficiency; Mitochondrial complex IV deficiency, nuclear type 3, OMIM:619046
Unexplained young onset end-stage renal disease - additional genes v0.1 CHRM3 Achchuthan Shanmugasundram gene: CHRM3 was added
gene: CHRM3 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: CHRM3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CHRM3 were set to 31441039; 10944224; 22077972
Phenotypes for gene: CHRM3 were set to Megacystis; Urinary Bladder Disease; Prune belly syndrome, OMIM:100100
Unexplained young onset end-stage renal disease - additional genes v0.1 CHD7 Achchuthan Shanmugasundram gene: CHD7 was added
gene: CHD7 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: CHD7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: CHD7 were set to CHARGE syndrome 214800
Unexplained young onset end-stage renal disease - additional genes v0.1 CHD1L Achchuthan Shanmugasundram gene: CHD1L was added
gene: CHD1L was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: CHD1L was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: CHD1L were set to 24429398; 22146311
Phenotypes for gene: CHD1L were set to ORPHA93545; Renal or urinary tract malformation (CAKUT)
Unexplained young onset end-stage renal disease - additional genes v0.1 BNC2 Achchuthan Shanmugasundram gene: BNC2 was added
gene: BNC2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,Other
Mode of inheritance for gene: BNC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: BNC2 were set to 31051115
Phenotypes for gene: BNC2 were set to Congenital lower urinary-tract obstruction; Posterior urethral valves; Lower urinary tract obstruction, congenital, 618612; PUV
Mode of pathogenicity for gene: BNC2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Unexplained young onset end-stage renal disease - additional genes v0.1 BMP4 Achchuthan Shanmugasundram gene: BMP4 was added
gene: BMP4 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: BMP4 was set to Unknown
Unexplained young onset end-stage renal disease - additional genes v0.1 BICC1 Achchuthan Shanmugasundram gene: BICC1 was added
gene: BICC1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: BICC1 was set to Unknown
Phenotypes for gene: BICC1 were set to {Renal dysplasia, cystic, susceptibility to}, 601331
Unexplained young onset end-stage renal disease - additional genes v0.1 ARMC9 Achchuthan Shanmugasundram gene: ARMC9 was added
gene: ARMC9 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: ARMC9 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ARMC9 were set to 28625504
Phenotypes for gene: ARMC9 were set to Joubert syndrome 30, 617622
Unexplained young onset end-stage renal disease - additional genes v0.1 ANOS1 Achchuthan Shanmugasundram gene: ANOS1 was added
gene: ANOS1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: ANOS1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: ANOS1 were set to 9719154; 11531922
Phenotypes for gene: ANOS1 were set to Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1); Kallman syndrome
Unexplained young onset end-stage renal disease - additional genes v0.1 AGTR1 Achchuthan Shanmugasundram gene: AGTR1 was added
gene: AGTR1 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: AGTR1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: AGTR1 were set to Renal tubular dysgenesis, 267430; Hypertension, essential, 145500; Renal Tubular Dysgenesis
Unexplained young onset end-stage renal disease - additional genes v0.1 AGT Achchuthan Shanmugasundram gene: AGT was added
gene: AGT was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: AGT was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: AGT were set to Renal tubular dysgenesis, 267430; Renal Tubular Dysgenesis; {Hypertension, essential, susceptibility to}, 145500{Preeclampsia, susceptibility to}Renal tubular dysgenesis, 267430
Unexplained young onset end-stage renal disease - additional genes v0.1 ACTG2 Achchuthan Shanmugasundram gene: ACTG2 was added
gene: ACTG2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: ACTG2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ACTG2 were set to PMID: 25998219
Phenotypes for gene: ACTG2 were set to Visceral myopathy (Megacystis-microcolon intestinal hypoperistalsis syndrome, Berdon syndrome) 155310; visceral myopathy; Berdon syndrome; Megacystis-microcolon intestinal hypoperistalsis syndrome
Unexplained young onset end-stage renal disease - additional genes v0.1 ACTA2 Achchuthan Shanmugasundram gene: ACTA2 was added
gene: ACTA2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Red
Mode of inheritance for gene: ACTA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: ACTA2 were set to Multi system smooth muscle dysfunction
Unexplained young onset end-stage renal disease - additional genes v0.1 ACE Achchuthan Shanmugasundram gene: ACE was added
gene: ACE was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: ACE was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ACE were set to {Myocardial infarction, susceptibility to}{Alzheimer disease, susceptibility to}, 104300{Microvascular complications of diabetes 3}, 612624[Angiotensin I-converting enzyme, benign serum increase]{SARS, progression of}Renal tubular; Renal Tubular Dysgenesis 267430; Renal Tubular Dysgenesis
Unexplained young onset end-stage renal disease - additional genes v0.0 Achchuthan Shanmugasundram Added Panel Unexplained young onset end-stage renal disease - additional genes
Set panel types to: GMS Rare Disease Virtual; Component Of Super Panel
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v1.4 Achchuthan Shanmugasundram Panel version 1.3 has been signed off on 2024-05-30
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v1.3 Achchuthan Shanmugasundram Panel signed off version 1.0 has been removed
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v1.2 Achchuthan Shanmugasundram Panel name changed from Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency – full ACADM sequencing to Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2024-05-29
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.3 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease; GMS signed-off
Diagnostic testing for Glutaric acidaemia I v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2024-05-29
Diagnostic testing for Glutaric acidaemia I v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Diagnostic testing for Isovaleric acidaemia v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2024-05-29
Diagnostic testing for Isovaleric acidaemia v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Diagnostic testing for Isovaleric acidaemia v0.6 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease; GMS signed-off
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.9 Achchuthan Shanmugasundram Panel version 2.8 has been signed off on 2024-05-29
NARP syndrome or maternally inherited Leigh syndrome v1.4 Achchuthan Shanmugasundram Panel version 1.3 has been signed off on 2024-05-29
NARP syndrome or maternally inherited Leigh syndrome v1.3 MT-ND6 Achchuthan Shanmugasundram Tag curated_removed tag was added to gene: MT-ND6.
NARP syndrome or maternally inherited Leigh syndrome v1.3 MT-ND6 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreyfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to grey following NHS Genomic Medicine Service approval.
NARP syndrome or maternally inherited Leigh syndrome v1.3 MT-ND6 Achchuthan Shanmugasundram edited their review of gene: MT-ND6: Added comment: The rating of this gene has been updated togreyfollowing NHS Genomic Medicine Service approval.; Changed rating: RED
NARP syndrome or maternally inherited Leigh syndrome v1.2 MT-ND6 Achchuthan Shanmugasundram Source Expert Review Removed was added to MT-ND6.
Rating Changed from Green List (high evidence) to No List (delete)
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 SLC25A11 Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: SLC25A11.
Tag Q4_23_NHS_review was removed from gene: SLC25A11.
Tag Q4_23_expert_review was removed from gene: SLC25A11.
Tag curated_removed tag was added to gene: SLC25A11.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 SLC25A11 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreyfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to grey following NHS Genomic Medicine Service approval.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 MDH2 Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: MDH2.
Tag Q4_23_NHS_review was removed from gene: MDH2.
Tag Q4_23_expert_review was removed from gene: MDH2.
Tag curated_removed tag was added to gene: MDH2.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 MDH2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreyfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to grey following NHS Genomic Medicine Service approval.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 DLST Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: DLST.
Tag Q4_23_NHS_review was removed from gene: DLST.
Tag Q4_23_expert_review was removed from gene: DLST.
Tag curated_removed tag was added to gene: DLST.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 DLST Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreyfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to grey following NHS Genomic Medicine Service approval.
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 DLST Achchuthan Shanmugasundram commented on gene: DLST
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 SLC25A11 Achchuthan Shanmugasundram commented on gene: SLC25A11
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.8 MDH2 Achchuthan Shanmugasundram commented on gene: MDH2
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.7 DLST Achchuthan Shanmugasundram Source Expert Review Removed was added to DLST.
Rating Changed from Green List (high evidence) to No List (delete)
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.7 SLC25A11 Achchuthan Shanmugasundram Source Expert Review Removed was added to SLC25A11.
Rating Changed from Green List (high evidence) to No List (delete)
Inherited phaeochromocytoma and paraganglioma excluding NF1 v2.7 MDH2 Achchuthan Shanmugasundram Source Expert Review Removed was added to MDH2.
Rating Changed from Green List (high evidence) to No List (delete)
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.2 ACADM Achchuthan Shanmugasundram Classified gene: ACADM as Green List (high evidence)
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.2 ACADM Achchuthan Shanmugasundram Gene: acadm has been classified as Green List (High Evidence).
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.1 ACADM Achchuthan Shanmugasundram reviewed gene: ACADM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Diagnostic testing for Isovaleric acidaemia v0.5 IVD Achchuthan Shanmugasundram reviewed gene: IVD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Diagnostic testing for Isovaleric acidaemia v0.4 IVD Achchuthan Shanmugasundram Source Expert Review Green was added to IVD.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Diagnostic testing for Glutaric acidaemia I v0.4 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease; GMS signed-off
Diagnostic testing for Glutaric acidaemia I v0.3 GCDH Achchuthan Shanmugasundram reviewed gene: GCDH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Diagnostic testing for Glutaric acidaemia I v0.2 GCDH Achchuthan Shanmugasundram Source Expert Review Green was added to GCDH.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.1 ACADM Achchuthan Shanmugasundram gene: ACADM was added
gene: ACADM was added to Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency – full ACADM sequencing. Sources: NHS GMS
Mode of inheritance for gene: ACADM was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ACADM were set to Acyl-CoA dehydrogenase, medium chain, deficiency of, OMIM:201450
Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency - full ACADM sequencing v0.0 Achchuthan Shanmugasundram Added Panel Diagnostic testing for MCADD - Medium-chain acyl-CoA dehydrogenase deficiency – full ACADM sequencing
Set list of related panels to R451
Set panel types to: GMS Rare Disease
Diagnostic testing for Glutaric acidaemia I v0.1 GCDH Achchuthan Shanmugasundram gene: GCDH was added
gene: GCDH was added to Diagnostic testing for Glutaric acidaemia I. Sources: NHS GMS
Mode of inheritance for gene: GCDH was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GCDH were set to Glutaricaciduria, type I, OMIM:231670
Diagnostic testing for Glutaric acidaemia I v0.0 Achchuthan Shanmugasundram Added Panel Diagnostic testing for Glutaric acidaemia I
Set list of related panels to R449
Set panel types to: GMS Rare Disease
Diagnostic testing for Isovaleric acidaemia v0.2 Achchuthan Shanmugasundram Panel name changed from Isovaleric acidaemia to Diagnostic testing for Isovaleric acidaemia
Diagnostic testing for Isovaleric acidaemia v0.1 IVD Achchuthan Shanmugasundram gene: IVD was added
gene: IVD was added to Isovaleric acidaemia. Sources: NHS GMS
Mode of inheritance for gene: IVD was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: IVD were set to Isovaleric acidemia, OMIM:243500
Diagnostic testing for Isovaleric acidaemia v0.0 Achchuthan Shanmugasundram Added Panel Isovaleric acidaemia
Set list of related panels to R450
Set panel types to: GMS Rare Disease
Congenital muscular dystrophy and congenital myopathy v1.2 GFER Arina Puzriakova Deleted their comment
Unexplained death in infancy and sudden unexplained death in childhood v9.39 Achchuthan Shanmugasundram Panel version 9.38 has been signed off on 2024-05-16
Unexplained death in infancy and sudden unexplained death in childhood v9.37 Achchuthan Shanmugasundram Panel signed off version 9.22 has been removed
Progressive cardiac conduction disease v2.9 Achchuthan Shanmugasundram Panel version 2.8 has been signed off on 2024-05-16
Dilated and arrhythmogenic cardiomyopathy v2.26 Achchuthan Shanmugasundram Panel version 2.25 has been signed off on 2024-05-16
Brugada syndrome and cardiac sodium channel disease v3.11 Achchuthan Shanmugasundram Panel version 3.10 has been signed off on 2024-05-16
Arrhythmogenic right ventricular cardiomyopathy v3.12 Achchuthan Shanmugasundram Panel version 3.11 has been signed off on 2024-05-16
Short QT syndrome v3.13 Achchuthan Shanmugasundram Panel version 3.12 has been signed off on 2024-05-16
Catecholaminergic polymorphic VT v4.7 Achchuthan Shanmugasundram Panel version 4.6 has been signed off on 2024-05-16
Hypertrophic cardiomyopathy v4.10 Achchuthan Shanmugasundram Panel version 4.9 has been signed off on 2024-05-16
Proteinuric renal disease v4.16 Achchuthan Shanmugasundram Panel version 4.15 has been signed off on 2024-05-16
Proteinuric renal disease v4.15 Achchuthan Shanmugasundram Panel signed off version 4.12 has been removed
Proteinuric renal disease v4.14 Achchuthan Shanmugasundram Panel types changed to Rare Disease 100K; GMS Rare Disease Virtual; GMS signed-off
Rare multisystem ciliopathy Super panel v15.10 Achchuthan Shanmugasundram Panel version 15.9 has been signed off on 2024-05-15
Other rare neuromuscular disorders v22.7 Eleanor Williams Panel signed off version 22.5 has been removed
Other rare neuromuscular disorders v22.6 Eleanor Williams Panel version 22.5 has been signed off on 2024-05-15
Paediatric disorders v45.60 Achchuthan Shanmugasundram Panel version 45.59 has been signed off on 2024-05-15
Paediatric disorders v45.59 Achchuthan Shanmugasundram Panel signed off version 45.38 has been removed
Hereditary ataxia and cerebellar anomalies - childhood onset v15.11 Eleanor Williams Panel version 15.10 has been signed off on 2024-05-15
Childhood onset leukodystrophy v19.31 Eleanor Williams Panel version 19.30 has been signed off on 2024-05-15
Other rare neuromuscular disorders v22.5 Achchuthan Shanmugasundram Panel version 22.4 has been signed off on 2024-05-15
Cerebral malformation v11.17 Eleanor Williams Panel version 11.16 has been signed off on 2024-05-15
Hypotonic infant v30.5 Achchuthan Shanmugasundram Panel version 30.4 has been signed off on 2024-05-15
Cystic renal disease v8.10 Eleanor Williams Panel version 8.9 has been signed off on 2024-05-15
Renal ciliopathies v3.7 Achchuthan Shanmugasundram Panel version 3.6 has been signed off on 2024-05-15
Monogenic short stature v1.2 Achchuthan Shanmugasundram Panel version 1.1 has been signed off on 2024-05-14
Monogenic short stature v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Monogenic short stature v0.174 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease Virtual; GMS Rare Disease; GMS signed-off
Congenital myaesthenic syndrome v4.7 Sarah Leigh Panel version 4.6 has been signed off on 2024-05-14
DDG2P v4.4 Sarah Leigh Panel version 4.3 has been signed off on 2024-05-14
Mosaic brain disorders - deep sequencing v1.2 Achchuthan Shanmugasundram Panel version 1.1 has been signed off on 2024-05-14
Long QT syndrome v3.9 Sarah Leigh Panel version 3.8 has been signed off on 2024-05-14
Mosaic brain disorders - deep sequencing v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Mosaic brain disorders - deep sequencing v0.147 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease; GMS signed-off
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v4.34 Sarah Leigh Panel version 4.33 has been signed off on 2024-05-14
Neurological ciliopathies v4.2 Sarah Leigh Panel version 4.1 has been signed off on 2024-05-14
Neurological segmental overgrowth v2.14 Sarah Leigh Panel version 2.13 has been signed off on 2024-05-14
Adult onset neurodegenerative disorder v5.5 Achchuthan Shanmugasundram Panel version 5.4 has been signed off on 2024-05-14
Paediatric motor neuronopathies v3.8 Sarah Leigh Panel version 3.7 has been signed off on 2024-05-14
Congenital muscular dystrophy and congenital myopathy v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2024-05-14
Congenital muscular dystrophy and congenital myopathy v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Ophthalmological ciliopathies v4.2 Sarah Leigh Panel version 4.1 has been signed off on 2024-05-14
Congenital muscular dystrophy and congenital myopathy v0.238 Achchuthan Shanmugasundram Panel types changed to GMS Rare Disease; Component Of Super Panel; GMS signed-off
Familial rhabdoid tumours v1.12 Achchuthan Shanmugasundram Panel version 1.11 has been signed off on 2024-05-14
Familial rhabdoid tumours v1.11 Achchuthan Shanmugasundram Panel signed off version 1.8 has been removed
Likely inborn error of metabolism v5.7 Achchuthan Shanmugasundram Panel version 5.6 has been signed off on 2024-05-14
Likely inborn error of metabolism v5.6 Achchuthan Shanmugasundram Panel signed off version 5.3 has been removed
Severe insulin resistance and lipodystrophy syndromes v4.57 Achchuthan Shanmugasundram Panel version 4.56 has been signed off on 2024-05-14
Early onset or syndromic epilepsy v5.11 Achchuthan Shanmugasundram Panel version 5.10 has been signed off on 2024-05-14
Distal myopathies v4.4 Achchuthan Shanmugasundram Panel version 4.3 has been signed off on 2024-05-14
Childhood onset hereditary spastic paraplegia v5.4 Achchuthan Shanmugasundram Panel version 5.3 has been signed off on 2024-05-14
Childhood onset dystonia, chorea or related movement disorder v4.4 Achchuthan Shanmugasundram Panel version 4.3 has been signed off on 2024-05-14
Cystic kidney disease v5.4 Sarah Leigh Panel version 5.3 has been signed off on 2024-05-14
Structural eye disease v3.80 Sarah Leigh Panel version 3.79 has been signed off on 2024-05-14
Monogenic hearing loss v4.43 Eleanor Williams Panel version 4.42 has been signed off on 2024-05-14
Retinal disorders v5.5 Sarah Leigh Panel version 5.4 has been signed off on 2024-05-14
Bilateral congenital or childhood onset cataracts v4.15 Sarah Leigh Panel version 4.14 has been signed off on 2024-05-14
Proteinuric renal disease v4.13 Eleanor Williams Panel version 4.12 has been signed off on 2024-05-14
Ataxia and cerebellar anomalies - narrow panel v5.4 Achchuthan Shanmugasundram Panel version 5.3 has been signed off on 2024-05-14
White matter disorders and cerebral calcification - narrow panel v4.4 Sarah Leigh Panel version 4.3 has been signed off on 2024-05-14
Arthrogryposis v6.4 Achchuthan Shanmugasundram Panel version 6.3 has been signed off on 2024-05-14
Severe microcephaly v5.8 Sarah Leigh Panel version 5.7 has been signed off on 2024-05-14
Rhabdomyolysis and metabolic muscle disorders v4.5 Sarah Leigh Panel version 4.4 has been signed off on 2024-05-14
Malformations of cortical development v5.5 Sarah Leigh Panel version 5.4 has been signed off on 2024-05-14
Adult onset neurodegenerative disorder v5.4 Achchuthan Shanmugasundram Panel version 5.3 has been signed off on 2024-05-14
Adult onset leukodystrophy v4.4 Achchuthan Shanmugasundram Panel version 4.3 has been signed off on 2024-05-14
Hydrocephalus v4.7 Sarah Leigh Panel version 4.6 has been signed off on 2024-05-14
Adult onset hereditary spastic paraplegia v4.5 Achchuthan Shanmugasundram Panel version 4.4 has been signed off on 2024-05-14
Holoprosencephaly - NOT chromosomal v4.12 Sarah Leigh Panel version 4.11 has been signed off on 2024-05-14
Holoprosencephaly - NOT chromosomal v4.11 Sarah Leigh Panel signed off version 4.9 has been removed
Adult onset hereditary spastic paraplegia v4.4 Achchuthan Shanmugasundram Panel version 4.3 has been signed off on 2024-05-14
Holoprosencephaly - NOT chromosomal v4.10 Sarah Leigh Panel version 4.9 has been signed off on 2024-05-14
Hereditary neuropathy or pain disorder v4.12 Sarah Leigh Panel version 4.11 has been signed off on 2024-05-14
Hereditary ataxia with onset in adulthood v5.4 Sarah Leigh Panel version 5.3 has been signed off on 2024-05-14
Adult onset dystonia, chorea or related movement disorder v3.20 Achchuthan Shanmugasundram Panel version 3.19 has been signed off on 2024-05-14
Skeletal dysplasia v5.4 Achchuthan Shanmugasundram Panel version 5.3 has been signed off on 2024-05-14
Congenital disorders of glycosylation v5.4 Sarah Leigh Panel version 5.3 has been signed off on 2024-05-14
Primary immunodeficiency or monogenic inflammatory bowel disease v5.4 Sarah Leigh Panel version 5.3 has been signed off on 2024-05-14
Skeletal ciliopathies v4.4 Achchuthan Shanmugasundram Panel version 4.3 has been signed off on 2024-05-14
Limb disorders v5.5 Achchuthan Shanmugasundram Panel version 5.4 has been signed off on 2024-05-14
Thalassaemia and other haemoglobinopathies v1.10 Sarah Leigh Panel version 1.9 has been signed off on 2024-05-14
Clefting v5.4 Achchuthan Shanmugasundram Panel version 5.3 has been signed off on 2024-05-14
Haemoglobinopathy trait or carrier testing v1.10 Sarah Leigh Panel version 1.9 has been signed off on 2024-05-14
Neonatal diabetes v4.7 Sarah Leigh Panel version 4.6 has been signed off on 2024-05-14
Severe insulin resistance and lipodystrophy syndromes v4.56 Achchuthan Shanmugasundram Panel signed off version 4.52 has been removed
Severe insulin resistance and lipodystrophy syndromes v4.55 Achchuthan Shanmugasundram Panel signed off version 4.52 has been removed
Mitochondrial disorders v6.5 Achchuthan Shanmugasundram Panel version 6.4 has been signed off on 2024-05-14
Paediatric disorders - additional genes v4.4 Sarah Leigh Panel version 4.3 has been signed off on 2024-05-14
Intellectual disability v6.14 Sarah Leigh Panel version 6.13 has been signed off on 2024-05-14
Inherited polyposis and early onset colorectal cancer - germline testing v2.12 Sarah Leigh Panel version 2.11 has been signed off on 2024-05-14
Paediatric or syndromic cardiomyopathy v4.4 Sarah Leigh Panel version 4.3 has been signed off on 2024-05-14
Unexplained young onset end-stage renal disease v4.5 Sarah Leigh Panel version 4.4 has been signed off on 2024-05-14
Unexplained death in infancy and sudden unexplained death in childhood v9.23 Sarah Leigh Panel version 9.22 has been signed off on 2024-05-14
Paediatric disorders v45.39 Sarah Leigh Panel version 45.38 has been signed off on 2024-05-14
Hypotonic infant v29.25 Sarah Leigh Panel version 29.24 has been signed off on 2024-05-14
Childhood onset leukodystrophy v19.24 Sarah Leigh Panel version 19.23 has been signed off on 2024-05-14
Familial rhabdoid tumours v1.10 Achchuthan Shanmugasundram List of related panels changed from R358; Rhabdoid tumour predisposition to R358; Rhabdoid tumour predisposition
Likely inborn error of metabolism v5.4 Sarah Leigh Panel name changed from Likely inborn error of metabolism - targeted testing not possible to Likely inborn error of metabolism
List of related panels changed from Likely inborn error of metabolism - targeted testing not possible; Likely inborn error of metabolism; Inborn errors of metabolism; R98 to Likely inborn error of metabolism - targeted testing not possible; Inborn errors of metabolism; R98
Panel version 5.3 has been signed off on 2024-05-14
Severe insulin resistance and lipodystrophy syndromes v4.54 Achchuthan Shanmugasundram List of related panels changed from R158;Lipodystrophy - childhood onset to R158; Lipodystrophy - childhood onset
Familial rhabdoid tumours v1.9 Sarah Leigh Panel name changed from Rhabdoid tumour predisposition to Familial rhabdoid tumours
List of related panels changed from R358 to R358; Rhabdoid tumour predisposition
Panel version 1.8 has been signed off on 2024-05-14
Severe insulin resistance and lipodystrophy syndromes v4.53 Sarah Leigh Panel name changed from Lipodystrophy - childhood onset to Severe insulin resistance and lipodystrophy syndromes
List of related panels changed from R158 to R158;Lipodystrophy - childhood onset
Panel version 4.52 has been signed off on 2024-05-14
Congenital muscular dystrophy and congenital myopathy v0.236 Achchuthan Shanmugasundram Panel types changed to GMS Rare Disease; Component Of Super Panel
Hypotonic infant v29.22 Achchuthan Shanmugasundram Changed child panels to: Intellectual disability; Likely inborn error of metabolism - targeted testing not possible; Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies; Congenital myaesthenic syndrome; Rhabdomyolysis and metabolic muscle disorders; Distal myopathies; Paediatric motor neuronopathies; Congenital muscular dystrophy and congenital myopathy
Other rare neuromuscular disorders v21.10 Achchuthan Shanmugasundram Changed child panels to: Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies; Congenital myaesthenic syndrome; Rhabdomyolysis and metabolic muscle disorders; Distal myopathies; Paediatric motor neuronopathies; Congenital muscular dystrophy and congenital myopathy
Congenital muscular dystrophy and congenital myopathy v0.235 Achchuthan Shanmugasundram Panel status changed from internal to public
Panel types changed to GMS Rare Disease; Component Of Super Panel; GMS signed-off
Hereditary neuropathy or pain disorder v4.11 RTN2 Sarah Leigh Tag Q2_24_NHS_review tag was added to gene: RTN2.
Hereditary neuropathy or pain disorder v4.11 SPTBN4 Sarah Leigh Tag Q2_24_promote_green was removed from gene: SPTBN4.
Tag Q2_24_NHS_review was removed from gene: SPTBN4.
Hereditary neuropathy or pain disorder v4.11 ABHD12 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: ABHD12.
Tag Q2_24_NHS_review tag was added to gene: ABHD12.
Hereditary neuropathy or pain disorder v4.11 AGXT Sarah Leigh Tag Q2_24_promote_green tag was added to gene: AGXT.
Tag Q2_24_NHS_review tag was added to gene: AGXT.
Hereditary neuropathy or pain disorder v4.11 APOA1 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: APOA1.
Tag Q2_24_NHS_review tag was added to gene: APOA1.
Hereditary neuropathy or pain disorder v4.11 B4GALNT1 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: B4GALNT1.
Tag Q2_24_NHS_review tag was added to gene: B4GALNT1.
Hereditary neuropathy or pain disorder v4.11 BCKDHB Sarah Leigh Tag Q2_24_promote_green tag was added to gene: BCKDHB.
Tag Q2_24_NHS_review tag was added to gene: BCKDHB.
Hereditary neuropathy or pain disorder v4.11 FXN Sarah Leigh Tag Q2_24_promote_green tag was added to gene: FXN.
Tag Q2_24_NHS_review tag was added to gene: FXN.
Hereditary neuropathy or pain disorder v4.11 GALC Sarah Leigh Tag Q2_24_promote_green tag was added to gene: GALC.
Tag Q2_24_NHS_review tag was added to gene: GALC.
Hereditary neuropathy or pain disorder v4.11 GBA2 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: GBA2.
Tag Q2_24_NHS_review tag was added to gene: GBA2.
Hereditary neuropathy or pain disorder v4.11 IARS2 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: IARS2.
Tag Q2_24_NHS_review tag was added to gene: IARS2.
Hereditary neuropathy or pain disorder v4.11 LYST Sarah Leigh Tag Q2_24_promote_green tag was added to gene: LYST.
Tag Q2_24_NHS_review tag was added to gene: LYST.
Hereditary neuropathy or pain disorder v4.11 MMACHC Sarah Leigh Tag Q2_24_promote_green tag was added to gene: MMACHC.
Tag Q2_24_NHS_review tag was added to gene: MMACHC.
Hereditary neuropathy or pain disorder v4.11 MTTP Sarah Leigh Tag Q2_24_promote_green tag was added to gene: MTTP.
Tag Q2_24_NHS_review tag was added to gene: MTTP.
Hereditary neuropathy or pain disorder v4.11 NAGA Sarah Leigh Tag Q2_24_promote_green tag was added to gene: NAGA.
Tag Q2_24_NHS_review tag was added to gene: NAGA.
Hereditary neuropathy or pain disorder v4.11 PDYN Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PDYN.
Tag Q2_24_NHS_review tag was added to gene: PDYN.
Hereditary neuropathy or pain disorder v4.11 PEX10 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PEX10.
Tag Q2_24_NHS_review tag was added to gene: PEX10.
Hereditary neuropathy or pain disorder v4.11 PEX7 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PEX7.
Tag Q2_24_NHS_review tag was added to gene: PEX7.
Hereditary neuropathy or pain disorder v4.11 PLP1 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PLP1.
Tag Q2_24_NHS_review tag was added to gene: PLP1.
Hereditary neuropathy or pain disorder v4.11 PMM2 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PMM2.
Tag Q2_24_NHS_review tag was added to gene: PMM2.
Hereditary neuropathy or pain disorder v4.11 PNPLA6 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: PNPLA6.
Tag Q2_24_NHS_review tag was added to gene: PNPLA6.
Hereditary neuropathy or pain disorder v4.11 POLR3A Sarah Leigh Tag Q2_24_promote_green tag was added to gene: POLR3A.
Tag Q2_24_NHS_review tag was added to gene: POLR3A.
Hereditary neuropathy or pain disorder v4.11 SACS Sarah Leigh Tag Q2_24_promote_green tag was added to gene: SACS.
Tag Q2_24_NHS_review tag was added to gene: SACS.
Hereditary neuropathy or pain disorder v4.11 SCARB2 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: SCARB2.
Tag Q2_24_NHS_review tag was added to gene: SCARB2.
Hereditary neuropathy or pain disorder v4.11 SLC25A19 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: SLC25A19.
Tag Q2_24_NHS_review tag was added to gene: SLC25A19.
Hereditary neuropathy or pain disorder v4.11 SPTBN4 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: SPTBN4.
Tag Q2_24_NHS_review tag was added to gene: SPTBN4.
Hereditary neuropathy or pain disorder v4.11 SURF1 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: SURF1.
Tag Q2_24_NHS_review tag was added to gene: SURF1.
Hereditary neuropathy or pain disorder v4.11 TYMP Sarah Leigh Tag Q2_24_promote_green tag was added to gene: TYMP.
Tag Q2_24_NHS_review tag was added to gene: TYMP.
Hereditary neuropathy or pain disorder v4.11 XK Sarah Leigh Tag Q2_24_promote_green tag was added to gene: XK.
Tag Q2_24_NHS_review tag was added to gene: XK.
Hereditary neuropathy or pain disorder v4.11 XK Sarah Leigh reviewed gene: XK: Rating: GREEN; Mode of pathogenicity: ; Publications: 8619554, 11261514; Phenotypes: McLeod syndrome, OMIM:300842; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Hereditary neuropathy or pain disorder v4.11 TYMP Sarah Leigh reviewed gene: TYMP: Rating: GREEN; Mode of pathogenicity: ; Publications: 14757860, 12177387, 9924029; Phenotypes: Mitochondrial DNA depletion syndrome 1 (MNGIE type), OMIM:603041; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 SURF1 Sarah Leigh reviewed gene: SURF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Charcot-Marie-Tooth disease, type 4K, OMIM:616684, Mitochondrial complex IV deficiency, nuclear type 1, OMIM:220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 SPTBN4 Sarah Leigh edited their review of gene: SPTBN4: Added comment: At least six SPTBN4 variants have been associated with OMIM:617519, which includes axonal and demyelinating peripheral neuropathy as one of the clinical features. Six SPTBN4 variants have been reported by PMID: 28540413;29861105 in five unrelated cases of OMIM:617519.; Changed rating: GREEN; Changed publications to: 28540413, 29861105; Changed phenotypes to: Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 SLC25A19 Sarah Leigh reviewed gene: SLC25A19: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), OMIM:613710; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 SCARB2 Sarah Leigh reviewed gene: SCARB2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 4, with or without renal failure, OMIM:254900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 SACS Sarah Leigh reviewed gene: SACS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Spastic ataxia, Charlevoix-Saguenay type, OMIM:270550; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 POLR3A Sarah Leigh reviewed gene: POLR3A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Wiedemann-Rautenstrauch syndrome, OMIM:264090, Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism OMIM:607694; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 PNPLA6 Sarah Leigh reviewed gene: PNPLA6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Oliver-McFarlane syndrome, OMIM:275400, Spastic paraplegia 39, autosomal recessive, OMIM:612020, Boucher-Neuhauser syndrome, OMIM:215470; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 PMM2 Sarah Leigh reviewed gene: PMM2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Ia, OMIM:212065; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 PLP1 Sarah Leigh reviewed gene: PLP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Spastic paraplegia 2, X-linked, OMIM:312920, Pelizaeus-Merzbacher disease, OMIM:312080; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Hereditary neuropathy or pain disorder v4.11 PEX7 Sarah Leigh reviewed gene: PEX7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Peroxisome biogenesis disorder 9B, OMIM:14879; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 PEX10 Sarah Leigh reviewed gene: PEX10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Peroxisome biogenesis disorder 6A (Zellweger), OMIM:614870, Peroxisome biogenesis disorder 6B, OMIM:614871; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 PDYN Sarah Leigh reviewed gene: PDYN: Rating: GREEN; Mode of pathogenicity: ; Publications: 21035104; Phenotypes: Spinocerebellar ataxia 23, OMIM:610245; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.11 NAGA Sarah Leigh reviewed gene: NAGA: Rating: GREEN; Mode of pathogenicity: ; Publications: 8782044, 11251574; Phenotypes: Kanzaki disease, OMIM:609242; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 MTTP Sarah Leigh reviewed gene: MTTP: Rating: GREEN; Mode of pathogenicity: ; Publications: 8361539, 10446076, 8111381; Phenotypes: Abetalipoproteinemia, OMIM:200100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 MMACHC Sarah Leigh reviewed gene: MMACHC: Rating: GREEN; Mode of pathogenicity: ; Publications: 17431913, 16311595, 19370762; Phenotypes: Methylmalonic aciduria and homocystinuria, cblC type, OMIM:277400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 LYST Sarah Leigh reviewed gene: LYST: Rating: GREEN; Mode of pathogenicity: ; Publications: 9215680, 8896560, 9215679, 11857544; Phenotypes: Chediak-Higashi syndrome, OMIM:214500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 IARS2 Sarah Leigh reviewed gene: IARS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia, OMIM:616007; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 GBA2 Sarah Leigh reviewed gene: GBA2: Rating: GREEN; Mode of pathogenicity: ; Publications: 24252062, 23332917, 23332916; Phenotypes: Spastic paraplegia 46, autosomal recessive, OMIM:614409; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 GALC Sarah Leigh reviewed gene: GALC: Rating: GREEN; Mode of pathogenicity: ; Publications: 20886637, 21070211; Phenotypes: Krabbe disease, OMIM:245200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 FXN Sarah Leigh reviewed gene: FXN: Rating: GREEN; Mode of pathogenicity: ; Publications: 21830088, 9737785, 8596916; Phenotypes: Friedreich ataxia, OMIM:229300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 BCKDHB Sarah Leigh reviewed gene: BCKDHB: Rating: GREEN; Mode of pathogenicity: ; Publications: 14742428, 2022752, 11509994; Phenotypes: Maple syrup urine disease, type Ib,OMIM:620698; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 B4GALNT1 Sarah Leigh reviewed gene: B4GALNT1: Rating: GREEN; Mode of pathogenicity: ; Publications: 23746551; Phenotypes: Spastic paraplegia 26, autosomal recessive, OMIM:609195; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 APOA1 Sarah Leigh reviewed gene: APOA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Amyloidosis, 3 or more types, OMIM:105200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.11 AGXT Sarah Leigh reviewed gene: AGXT: Rating: GREEN; Mode of pathogenicity: ; Publications: 1961759, 10960483, 15464418; Phenotypes: Hyperoxaluria, primary, type 1, OMIM:259900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.11 ABHD12 Sarah Leigh reviewed gene: ABHD12: Rating: GREEN; Mode of pathogenicity: ; Publications: 20797687, 24697911; Phenotypes: Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, OMIM:612674; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Adult onset hereditary spastic paraplegia v4.3 SPG7 Eleanor Williams Tag Q2_23_MOI was removed from gene: SPG7.
Hereditary neuropathy or pain disorder v4.10 SLC12A6 Eleanor Williams Tag for-review was removed from gene: SLC12A6.
Tag to_be_confirmed_NHSE was removed from gene: SLC12A6.
Tag Q4_23_promote_green was removed from gene: SLC12A6.
Tag Q4_23_NHS_review was removed from gene: SLC12A6.
Intellectual disability v6.13 ZBTB47 Eleanor Williams Tag gene-checked tag was added to gene: ZBTB47.
Intellectual disability v6.13 KDM5A Eleanor Williams Phenotypes for gene: KDM5A were changed from autism spectrum disorder, MONDO:0005258; intellectual disability, MONDO:0001071 to autism spectrum disorder, MONDO:0005258; intellectual disability, MONDO:0001071; El Hayek-Chahrour neurodevelopmental syndrome, OMIM:620820
Intellectual disability v6.12 KDM5A Eleanor Williams Tag gene-checked was removed from gene: KDM5A.
Mosaic brain disorders - deep sequencing v0.146 Eleanor Williams Panel status changed from public to internal
Monogenic short stature v0.173 Eleanor Williams Panel status changed from public to internal
Congenital muscular dystrophy and congenital myopathy v0.234 Eleanor Williams Panel status changed from public to internal
Mosaic brain disorders - deep sequencing v0.145 Eleanor Williams Panel status changed from internal to public
Monogenic short stature v0.172 Eleanor Williams Panel status changed from internal to public
Congenital muscular dystrophy and congenital myopathy v0.233 Eleanor Williams Panel status changed from internal to public
Early onset or syndromic epilepsy v5.10 ZBTB47 Eleanor Williams Tag gene-checked tag was added to gene: ZBTB47.
Intellectual disability v6.12 TMEM63B Eleanor Williams Tag gene-checked tag was added to gene: TMEM63B.
Early onset or syndromic epilepsy v5.10 TMEM63B Eleanor Williams Tag gene-checked tag was added to gene: TMEM63B.
Childhood onset dystonia, chorea or related movement disorder v4.3 TMEM151A Eleanor Williams Tag gene-checked tag was added to gene: TMEM151A.
Ataxia and cerebellar anomalies - narrow panel v5.3 THG1L Eleanor Williams Tag gene-checked tag was added to gene: THG1L.
Intellectual disability v6.12 PPP1R3F Eleanor Williams Tag gene-checked tag was added to gene: PPP1R3F.
Early onset or syndromic epilepsy v5.10 PPP1R3F Eleanor Williams Tag gene-checked tag was added to gene: PPP1R3F.
Intellectual disability v6.12 MAST4 Eleanor Williams Tag gene-checked tag was added to gene: MAST4.
Early onset or syndromic epilepsy v5.10 MAST4 Eleanor Williams Tag gene-checked tag was added to gene: MAST4.
Retinal disorders v5.4 CFAP20 Eleanor Williams Tag gene-checked tag was added to gene: CFAP20.
Paediatric or syndromic cardiomyopathy v4.3 CAP2 Eleanor Williams Tag gene-checked tag was added to gene: CAP2.
Early onset or syndromic epilepsy v5.10 RAB5C Eleanor Williams Tag gene-checked tag was added to gene: RAB5C.
Intellectual disability v6.12 RAB5C Eleanor Williams Tag gene-checked tag was added to gene: RAB5C.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 PTPN2 Eleanor Williams Tag gene-checked tag was added to gene: PTPN2.
Intellectual disability v6.12 PABPC1 Eleanor Williams Tag gene-checked tag was added to gene: PABPC1.
Early onset or syndromic epilepsy v5.10 PABPC1 Eleanor Williams Tag gene-checked tag was added to gene: PABPC1.
Neonatal diabetes v4.6 ONECUT1 Eleanor Williams Tag gene-checked tag was added to gene: ONECUT1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 NFAT5 Eleanor Williams Tag gene-checked tag was added to gene: NFAT5.
Intellectual disability v6.12 MYH10 Eleanor Williams Tag gene-checked tag was added to gene: MYH10.
Inherited polyposis and early onset colorectal cancer - germline testing v2.11 GREM1 Eleanor Williams Tag gene-checked tag was added to gene: GREM1.
Severe insulin resistance and lipodystrophy syndromes v4.52 EPHX1 Eleanor Williams Tag gene-checked tag was added to gene: EPHX1.
Adult onset neurodegenerative disorder v5.3 DNAJC7 Eleanor Williams Tag gene-checked tag was added to gene: DNAJC7.
Adult onset neurodegenerative disorder v5.3 DNAJC7 Eleanor Williams reviewed gene: DNAJC7: Rating: ; Mode of pathogenicity: None; Publications: 31768050, 35039179, 34233860, 32897108, 37870677, 35456894; Phenotypes: ; Mode of inheritance: None
Hereditary neuropathy or pain disorder v4.10 DHX9 Eleanor Williams Tag gene-checked tag was added to gene: DHX9.
Intellectual disability v6.12 DHX9 Eleanor Williams Tag gene-checked tag was added to gene: DHX9.
Intellectual disability v6.12 CNOT9 Eleanor Williams Tag gene-checked tag was added to gene: CNOT9.
Early onset or syndromic epilepsy v5.10 CNOT9 Eleanor Williams Tag gene-checked tag was added to gene: CNOT9.
Unexplained young onset end-stage renal disease v4.3 CFHR2 Eleanor Williams Tag gene-checked tag was added to gene: CFHR2.
Intellectual disability v6.12 CDK16 Eleanor Williams Tag gene-checked tag was added to gene: CDK16.
Structural eye disease v3.79 ARHGAP35 Eleanor Williams Tag gene-checked tag was added to gene: ARHGAP35.
Intellectual disability v6.12 ARF3 Eleanor Williams Tag gene-checked tag was added to gene: ARF3.
Early onset or syndromic epilepsy v5.10 ARF3 Eleanor Williams Tag gene-checked tag was added to gene: ARF3.
Severe microcephaly v5.7 ARF3 Eleanor Williams Tag gene-checked tag was added to gene: ARF3.
Clefting v5.3 AMOTL1 Eleanor Williams Tag gene-checked tag was added to gene: AMOTL1.
Congenital muscular dystrophy and congenital myopathy v0.232 ASCC3 Eleanor Williams Tag gene-checked was removed from gene: ASCC3.
Congenital muscular dystrophy and congenital myopathy v0.232 ASCC3 Eleanor Williams Phenotypes for gene: ASCC3 were changed from Congenital myopathy, MONDO:0019952 to Congenital myopathy, MONDO:0019952; Intellectual developmental disorder, autosomal recessive 81, OMIM:620700
Likely inborn error of metabolism v5.3 ATP5E Eleanor Williams Tag new-gene-name tag was added to gene: ATP5E.
Monogenic short stature v0.171 Eleanor Williams Panel status changed from public to internal
Mosaic brain disorders - deep sequencing v0.144 Eleanor Williams Panel status changed from public to internal
Congenital muscular dystrophy and congenital myopathy v0.231 Eleanor Williams Panel status changed from public to internal
Hereditary neuropathy or pain disorder v4.10 SLC12A6 Eleanor Williams commented on gene: SLC12A6
Hereditary neuropathy or pain disorder v4.10 SLC12A6 Eleanor Williams Mode of inheritance for gene: SLC12A6 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mosaic brain disorders - deep sequencing v0.143 Eleanor Williams Panel status changed from internal to public
Monogenic short stature v0.170 Eleanor Williams Panel status changed from internal to public
Congenital muscular dystrophy and congenital myopathy v0.230 Eleanor Williams Panel status changed from internal to public
Hereditary neuropathy or pain disorder v4.9 SURF1 Sarah Leigh Publications for gene: SURF1 were set to
Intellectual disability v6.12 MAST3 Sarah Leigh Tag Q2_24_NHS_review tag was added to gene: MAST3.
Early onset or syndromic epilepsy v5.10 MAST3 Sarah Leigh Tag Q2_24_NHS_review tag was added to gene: MAST3.
Intellectual disability v6.12 MAST3 Sarah Leigh Tag Q2_24_MOI was removed from gene: MAST3.
Intellectual disability v6.12 MAST3 Sarah Leigh Entity copied from Early onset or syndromic epilepsy v5.10
Intellectual disability v6.12 MAST3 Sarah Leigh gene: MAST3 was added
gene: MAST3 was added to Intellectual disability. Sources: Expert Review Amber,Literature
Q2_24_promote_green, Q2_24_MOI tags were added to gene: MAST3.
Mode of inheritance for gene: MAST3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: MAST3 were set to 34185323; 35095415
Mode of pathogenicity for gene: MAST3 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Early onset or syndromic epilepsy v5.10 MAST3 Sarah Leigh changed review comment from: MAST3 variants have been associated with Developmental and epileptic encephalopathy 108 (OMIM:620115). PMID:34185323 reports five de novo missense MAST3 variants in eleven unrelated individuals with developmental and epileptic encephalopathy, with a range of seizure types. Functional studies suggest that the MAST3 variants have a gain-of-function effect.
Sources: Literature; to: MAST3 variants have been associated with Developmental and epileptic encephalopathy 108 (OMIM:620115). PMID:34185323 reports five de novo missense MAST3 variants in eleven unrelated individuals with developmental and epileptic encephalopathy, with a range of seizure types. These variants are within the serine-threonine kinases (STK) domain. PMID: 35095415 reports a further four de novo missense MAST3 variants, within the domain of unknown function (DUF). It would appear that the variants within the STK domain are associated with a neurodevelopmental disorder with a epilepsy phenotype, while variants within the DUF domain have a autistic spectrum disorder phenotype (PMID: 35095415)
Functional studies suggest that the MAST3 variants have a gain-of-function effect (PMID:34185323; 35095415).
Early onset or syndromic epilepsy v5.10 MAST3 Sarah Leigh Publications for gene: MAST3 were set to 34185323
Early onset or syndromic epilepsy v5.9 MAST3 Sarah Leigh Added comment: Comment on mode of pathogenicity: It would appear that MAST3 variants have a gain-of-function effect (PMID:34185323).
Early onset or syndromic epilepsy v5.9 MAST3 Sarah Leigh Mode of pathogenicity for gene: MAST3 was changed from Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Early onset or syndromic epilepsy v5.8 MAST3 Sarah Leigh Classified gene: MAST3 as Amber List (moderate evidence)
Early onset or syndromic epilepsy v5.8 MAST3 Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Early onset or syndromic epilepsy v5.8 MAST3 Sarah Leigh Gene: mast3 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy v5.7 MAST3 Sarah Leigh Tag Q2_24_promote_green tag was added to gene: MAST3.
Tag Q2_24_MOI tag was added to gene: MAST3.
Early onset or syndromic epilepsy v5.7 MAST3 Sarah Leigh gene: MAST3 was added
gene: MAST3 was added to Early onset or syndromic epilepsy. Sources: Literature
Mode of inheritance for gene: MAST3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: MAST3 were set to 34185323
Mode of pathogenicity for gene: MAST3 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Review for gene: MAST3 was set to GREEN
Added comment: MAST3 variants have been associated with Developmental and epileptic encephalopathy 108 (OMIM:620115). PMID:34185323 reports five de novo missense MAST3 variants in eleven unrelated individuals with developmental and epileptic encephalopathy, with a range of seizure types. Functional studies suggest that the MAST3 variants have a gain-of-function effect.
Sources: Literature
Paediatric or syndromic cardiomyopathy v4.3 NEXN Hannah Robinson reviewed gene: NEXN: Rating: ; Mode of pathogenicity: None; Publications: 35166435, 33949776, 33027564, 32058062; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal; Current diagnostic: yes
Limb disorders v5.4 FBXW11 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 SLC5A6 Eleanor Williams changed review comment from: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remainsred.; to: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remains red.
Early onset or syndromic epilepsy v5.6 ZBTB47 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 U2AF2 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 TRIT1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 TMEM63B Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 SHQ1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 SHQ1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 SCN8A Eleanor Williams changed review comment from: The mode of inheritance of this gene has been updated to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 RAB5C Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PTCD3 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PPP1R3F Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'X-LINKED: hemizygous mutation in males, biallelic mutations in females'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, biallelic mutations in females' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PLA2G6 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PIP5K1C Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PIGM Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 PABPC1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 MAST4 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 LETM1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 KDM6B Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 KCNH5 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 HECTD4 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ESAM Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 EIF4A2 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 DNAJC6 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 CRELD1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ATP6V0C Eleanor Williams changed review comment from: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ASL Eleanor Williams changed review comment from: The rating of this gene has been updated to green and the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ARF3 Eleanor Williams changed review comment from: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 AGO1 Eleanor Williams changed review comment from: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 CNOT9 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ATP6V0C Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ASL Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 ARF3 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 AGO1 Eleanor Williams changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v5.6 CACNB4 Eleanor Williams edited their review of gene: CACNB4: Changed rating: RED
Early onset or syndromic epilepsy v5.6 CACNB4 Eleanor Williams changed review comment from: The rating of this gene has been updated from green to redfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated from green to red following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 RETREG1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RETREG1.
Tag Q4_23_NHS_review was removed from gene: RETREG1.
Childhood onset hereditary spastic paraplegia v5.3 RETREG1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 PPFIBP1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 PPFIBP1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PPFIBP1.
Childhood onset hereditary spastic paraplegia v5.3 HECTD4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HECTD4.
Childhood onset hereditary spastic paraplegia v5.3 HECTD4 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 CLDN11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLDN11.
Childhood onset hereditary spastic paraplegia v5.3 CLDN11 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 UCHL1 Achchuthan Shanmugasundram Tag Q3_23_MOI was removed from gene: UCHL1.
Childhood onset hereditary spastic paraplegia v5.3 UCHL1 Achchuthan Shanmugasundram changed review comment from: The mode of inheritance of this gene has been updated toBOTH monoallelic and biallelic, autosomal or pseudoautosomalfollowing NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 LETM1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Childhood onset hereditary spastic paraplegia v5.3 AMFR Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: AMFR.
Childhood onset hereditary spastic paraplegia v5.3 AMFR Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 UCHL1 Achchuthan Shanmugasundram reviewed gene: UCHL1: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Childhood onset hereditary spastic paraplegia v5.3 RETREG1 Achchuthan Shanmugasundram commented on gene: RETREG1: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 PPFIBP1 Achchuthan Shanmugasundram commented on gene: PPFIBP1: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 LETM1 Achchuthan Shanmugasundram reviewed gene: LETM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Childhood onset hereditary spastic paraplegia v5.3 HECTD4 Achchuthan Shanmugasundram commented on gene: HECTD4: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 CLDN11 Achchuthan Shanmugasundram commented on gene: CLDN11: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.3 AMFR Achchuthan Shanmugasundram commented on gene: AMFR: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset hereditary spastic paraplegia v5.2 UCHL1 Achchuthan Shanmugasundram Mode of inheritance for gene UCHL1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Childhood onset hereditary spastic paraplegia v5.2 RETREG1 Achchuthan Shanmugasundram Source Expert Review Green was added to RETREG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset hereditary spastic paraplegia v5.2 PPFIBP1 Achchuthan Shanmugasundram Source NHS GMS was added to PPFIBP1.
Source Expert Review Green was added to PPFIBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset hereditary spastic paraplegia v5.2 LETM1 Achchuthan Shanmugasundram Source NHS GMS was added to LETM1.
Source Expert Review Green was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset hereditary spastic paraplegia v5.2 HECTD4 Achchuthan Shanmugasundram Source Expert Review Green was added to HECTD4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset hereditary spastic paraplegia v5.2 CLDN11 Achchuthan Shanmugasundram Source NHS GMS was added to CLDN11.
Source Expert Review Green was added to CLDN11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset hereditary spastic paraplegia v5.2 AMFR Achchuthan Shanmugasundram Source NHS GMS was added to AMFR.
Source Expert Review Green was added to AMFR.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.3 AFG3L2 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: AFG3L2.
Childhood onset dystonia, chorea or related movement disorder v4.3 AFG3L2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated from green toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated from green to amber following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SHQ1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SHQ1.
Childhood onset dystonia, chorea or related movement disorder v4.3 SHQ1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 ASL Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ASL.
Tag Q4_23_NHS_review was removed from gene: ASL.
Childhood onset dystonia, chorea or related movement disorder v4.3 ASL Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 ARX Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ARX.
Childhood onset dystonia, chorea or related movement disorder v4.3 ARX Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 OCLN Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: OCLN.
Tag Q3_23_demote_red was removed from gene: OCLN.
Childhood onset dystonia, chorea or related movement disorder v4.3 OCLN Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated from green toredfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated from green to red following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 TSPOAP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TSPOAP1.
Childhood onset dystonia, chorea or related movement disorder v4.3 TSPOAP1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 TMEM151A Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 TMEM151A Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TMEM151A.
Tag Q3_23_NHS_review was removed from gene: TMEM151A.
Childhood onset dystonia, chorea or related movement disorder v4.3 TBC1D24 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TBC1D24.
Childhood onset dystonia, chorea or related movement disorder v4.3 TBC1D24 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SYT1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SYT1.
Childhood onset dystonia, chorea or related movement disorder v4.3 SYT1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SQSTM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SQSTM1.
Childhood onset dystonia, chorea or related movement disorder v4.3 SQSTM1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC30A9 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC30A9.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC30A9 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC18A2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC18A2.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC18A2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 L2HGDH Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: L2HGDH.
Childhood onset dystonia, chorea or related movement disorder v4.3 L2HGDH Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 KCNQ2 Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: KCNQ2.
Tag Q3_23_demote_red was removed from gene: KCNQ2.
Childhood onset dystonia, chorea or related movement disorder v4.3 DNAJC6 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DNAJC6.
Childhood onset dystonia, chorea or related movement disorder v4.3 DNAJC6 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 KCNQ2 Achchuthan Shanmugasundram commented on gene: KCNQ2
Childhood onset dystonia, chorea or related movement disorder v4.3 TSPOAP1 Achchuthan Shanmugasundram reviewed gene: TSPOAP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v4.3 TMEM151A Achchuthan Shanmugasundram commented on gene: TMEM151A: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 TBC1D24 Achchuthan Shanmugasundram commented on gene: TBC1D24: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SYT1 Achchuthan Shanmugasundram commented on gene: SYT1: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SQSTM1 Achchuthan Shanmugasundram commented on gene: SQSTM1: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC30A9 Achchuthan Shanmugasundram commented on gene: SLC30A9: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SLC18A2 Achchuthan Shanmugasundram commented on gene: SLC18A2: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 SHQ1 Achchuthan Shanmugasundram reviewed gene: SHQ1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v4.3 OCLN Achchuthan Shanmugasundram reviewed gene: OCLN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Childhood onset dystonia, chorea or related movement disorder v4.3 L2HGDH Achchuthan Shanmugasundram commented on gene: L2HGDH: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Childhood onset dystonia, chorea or related movement disorder v4.3 DNAJC6 Achchuthan Shanmugasundram reviewed gene: DNAJC6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v4.3 ASL Achchuthan Shanmugasundram reviewed gene: ASL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Childhood onset dystonia, chorea or related movement disorder v4.3 ARX Achchuthan Shanmugasundram reviewed gene: ARX: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Childhood onset dystonia, chorea or related movement disorder v4.3 AFG3L2 Achchuthan Shanmugasundram reviewed gene: AFG3L2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Childhood onset dystonia, chorea or related movement disorder v4.2 TSPOAP1 Achchuthan Shanmugasundram Source Expert Review Green was added to TSPOAP1.
Source NHS GMS was added to TSPOAP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 TMEM151A Achchuthan Shanmugasundram Source Expert Review Green was added to TMEM151A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 TBC1D24 Achchuthan Shanmugasundram Source Expert Review Green was added to TBC1D24.
Source NHS GMS was added to TBC1D24.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 SYT1 Achchuthan Shanmugasundram Source Expert Review Green was added to SYT1.
Source NHS GMS was added to SYT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 SQSTM1 Achchuthan Shanmugasundram Source Expert Review Green was added to SQSTM1.
Source NHS GMS was added to SQSTM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 SLC30A9 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC30A9.
Source NHS GMS was added to SLC30A9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 SLC18A2 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC18A2.
Source NHS GMS was added to SLC18A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 SHQ1 Achchuthan Shanmugasundram Source Expert Review Green was added to SHQ1.
Source NHS GMS was added to SHQ1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 OCLN Achchuthan Shanmugasundram Source Expert Review Red was added to OCLN.
Source NHS GMS was added to OCLN.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 L2HGDH Achchuthan Shanmugasundram Source Expert Review Green was added to L2HGDH.
Source NHS GMS was added to L2HGDH.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 DNAJC6 Achchuthan Shanmugasundram Source Expert Review Green was added to DNAJC6.
Source NHS GMS was added to DNAJC6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 ASL Achchuthan Shanmugasundram Source Expert Review Green was added to ASL.
Source NHS GMS was added to ASL.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 ARX Achchuthan Shanmugasundram Source Expert Review Green was added to ARX.
Source NHS GMS was added to ARX.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Childhood onset dystonia, chorea or related movement disorder v4.2 AFG3L2 Achchuthan Shanmugasundram Source NHS GMS was added to AFG3L2.
Source Expert Review Amber was added to AFG3L2.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Arthrogryposis v6.3 ACTC1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ACTC1.
Arthrogryposis v6.3 ACTC1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Arthrogryposis v6.3 ACTC1 Achchuthan Shanmugasundram commented on gene: ACTC1: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Arthrogryposis v6.2 ACTC1 Achchuthan Shanmugasundram Source NHS GMS was added to ACTC1.
Source Expert Review Green was added to ACTC1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset leukodystrophy v4.3 RNASET2 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: RNASET2.
Adult onset leukodystrophy v4.3 RNASET2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 POLR1C Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: POLR1C.
Adult onset leukodystrophy v4.3 POLR1C Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 MARS Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: MARS.
Adult onset leukodystrophy v4.3 MARS Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 COL4A2 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: COL4A2.
Adult onset leukodystrophy v4.3 AARS Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: AARS.
Adult onset leukodystrophy v4.3 OCRL Achchuthan Shanmugasundram Tag Q4_23_demote_amber was removed from gene: OCRL.
Tag Q4_23_expert_review was removed from gene: OCRL.
Adult onset leukodystrophy v4.3 OCRL Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 HMGCL Achchuthan Shanmugasundram Tag Q4_23_demote_amber was removed from gene: HMGCL.
Tag Q4_23_expert_review was removed from gene: HMGCL.
Adult onset leukodystrophy v4.3 HMGCL Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 RPS6KA3 Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: RPS6KA3.
Tag Q3_23_demote_red was removed from gene: RPS6KA3.
Adult onset leukodystrophy v4.3 RPS6KA3 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toredfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to red following NHS Genomic Medicine Service approval.
Adult onset leukodystrophy v4.3 RNF216 Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: RNF216.
Tag Q3_23_demote_amber was removed from gene: RNF216.
Adult onset leukodystrophy v4.3 GCDH Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: GCDH.
Tag Q3_23_MOI was removed from gene: GCDH.
Adult onset leukodystrophy v4.3 GCDH Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated to greenand the mode of inheritance set to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Adult onset neurodegenerative disorder v5.3 DNAJC7 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: DNAJC7.
Adult onset neurodegenerative disorder v5.3 GBA Achchuthan Shanmugasundram reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Adult onset neurodegenerative disorder v5.3 DNAJC7 Achchuthan Shanmugasundram reviewed gene: DNAJC7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Adult onset leukodystrophy v4.3 RPS6KA3 Achchuthan Shanmugasundram reviewed gene: RPS6KA3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 RNF216 Achchuthan Shanmugasundram commented on gene: RNF216
Adult onset leukodystrophy v4.3 RNASET2 Achchuthan Shanmugasundram reviewed gene: RNASET2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 POLR1C Achchuthan Shanmugasundram reviewed gene: POLR1C: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 OCRL Achchuthan Shanmugasundram reviewed gene: OCRL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 MARS Achchuthan Shanmugasundram reviewed gene: MARS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 HMGCL Achchuthan Shanmugasundram reviewed gene: HMGCL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset leukodystrophy v4.3 COL4A2 Achchuthan Shanmugasundram commented on gene: COL4A2
Adult onset leukodystrophy v4.3 AARS Achchuthan Shanmugasundram commented on gene: AARS
Adult onset leukodystrophy v4.3 GCDH Achchuthan Shanmugasundram reviewed gene: GCDH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Adult onset neurodegenerative disorder v5.2 GBA Achchuthan Shanmugasundram Source Expert Review Green was added to GBA.
Mode of inheritance for gene GBA was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset neurodegenerative disorder v5.2 DNAJC7 Achchuthan Shanmugasundram Source NHS GMS was added to DNAJC7.
Source Expert Review Green was added to DNAJC7.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset leukodystrophy v4.2 RPS6KA3 Achchuthan Shanmugasundram Source Expert Review Red was added to RPS6KA3.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Adult onset leukodystrophy v4.2 RNASET2 Achchuthan Shanmugasundram Source Expert Review Amber was added to RNASET2.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset leukodystrophy v4.2 POLR1C Achchuthan Shanmugasundram Source Expert Review Amber was added to POLR1C.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset leukodystrophy v4.2 OCRL Achchuthan Shanmugasundram Source Expert Review Amber was added to OCRL.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset leukodystrophy v4.2 MARS Achchuthan Shanmugasundram Source Expert Review Amber was added to MARS.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset leukodystrophy v4.2 HMGCL Achchuthan Shanmugasundram Source Expert Review Amber was added to HMGCL.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset leukodystrophy v4.2 GCDH Achchuthan Shanmugasundram Source NHS GMS was added to GCDH.
Source Expert Review Green was added to GCDH.
Mode of inheritance for gene GCDH was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset hereditary spastic paraplegia v4.3 UCHL1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: UCHL1.
Tag Q3_23_MOI was removed from gene: UCHL1.
Adult onset hereditary spastic paraplegia v4.3 UCHL1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Adult onset hereditary spastic paraplegia v4.3 PRNP Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PRNP.
Adult onset hereditary spastic paraplegia v4.3 PRNP Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Adult onset hereditary spastic paraplegia v4.3 AP4S1 Achchuthan Shanmugasundram Tag for-review was removed from gene: AP4S1.
Tag to_be_confirmed_NHSE was removed from gene: AP4S1.
Adult onset hereditary spastic paraplegia v4.3 AP4S1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.
Adult onset hereditary spastic paraplegia v4.3 AP4M1 Achchuthan Shanmugasundram Tag for-review was removed from gene: AP4M1.
Tag to_be_confirmed_NHSE was removed from gene: AP4M1.
Adult onset hereditary spastic paraplegia v4.3 AP4M1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.
Adult onset hereditary spastic paraplegia v4.3 AP4B1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.
Adult onset hereditary spastic paraplegia v4.3 AP4E1 Achchuthan Shanmugasundram Tag for-review was removed from gene: AP4E1.
Tag to_be_confirmed_NHSE was removed from gene: AP4E1.
Adult onset hereditary spastic paraplegia v4.3 AP4E1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.
Adult onset hereditary spastic paraplegia v4.3 AP4B1 Achchuthan Shanmugasundram Tag for-review was removed from gene: AP4B1.
Tag to_be_confirmed_NHSE was removed from gene: AP4B1.
Adult onset hereditary spastic paraplegia v4.3 AP4B1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toamberfollowing NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.; to: The rating of this gene has been updated to amber following NHS Genomic Medicine Service approval. The associated phenotype has childhood onset.
Adult onset hereditary spastic paraplegia v4.3 UCHL1 Achchuthan Shanmugasundram reviewed gene: UCHL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Adult onset hereditary spastic paraplegia v4.3 PRNP Achchuthan Shanmugasundram reviewed gene: PRNP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Adult onset hereditary spastic paraplegia v4.3 AP4S1 Achchuthan Shanmugasundram reviewed gene: AP4S1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset hereditary spastic paraplegia v4.3 AP4M1 Achchuthan Shanmugasundram reviewed gene: AP4M1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset hereditary spastic paraplegia v4.3 AP4E1 Achchuthan Shanmugasundram reviewed gene: AP4E1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset hereditary spastic paraplegia v4.3 AP4B1 Achchuthan Shanmugasundram reviewed gene: AP4B1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Adult onset hereditary spastic paraplegia v4.2 UCHL1 Achchuthan Shanmugasundram Source Expert Review Green was added to UCHL1.
Mode of inheritance for gene UCHL1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset hereditary spastic paraplegia v4.2 PRNP Achchuthan Shanmugasundram Source Expert Review Green was added to PRNP.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Adult onset hereditary spastic paraplegia v4.2 AP4S1 Achchuthan Shanmugasundram Source Expert Review Amber was added to AP4S1.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset hereditary spastic paraplegia v4.2 AP4M1 Achchuthan Shanmugasundram Source Expert Review Amber was added to AP4M1.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset hereditary spastic paraplegia v4.2 AP4E1 Achchuthan Shanmugasundram Source Expert Review Amber was added to AP4E1.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset hereditary spastic paraplegia v4.2 AP4B1 Achchuthan Shanmugasundram Source Expert Review Amber was added to AP4B1.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Adult onset dystonia, chorea or related movement disorder v3.19 GBA Achchuthan Shanmugasundram reviewed gene: GBA: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Adult onset dystonia, chorea or related movement disorder v3.19 GBA Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: GBA.
Adult onset dystonia, chorea or related movement disorder v3.19 GBA Achchuthan Shanmugasundram Mode of inheritance for gene GBA was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Skeletal dysplasia v5.3 TNFRSF11A Achchuthan Shanmugasundram Tag for-review was removed from gene: TNFRSF11A.
Tag to_be_confirmed_NHSE was removed from gene: TNFRSF11A.
Skeletal dysplasia v5.3 TNFRSF11A Achchuthan Shanmugasundram changed review comment from: The mode of inheritance of this gene has been updated to'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 ANAPC1 Achchuthan Shanmugasundram Tag for-review was removed from gene: ANAPC1.
Tag to_be_confirmed_NHSE was removed from gene: ANAPC1.
Skeletal dysplasia v5.3 ANAPC1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 UBA2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 UBA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: UBA2.
Tag Q4_23_NHS_review was removed from gene: UBA2.
Skeletal dysplasia v5.3 PSMC3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PSMC3.
Skeletal dysplasia v5.3 PSMC3 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 ERI1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 FBXW11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FBXW11.
Tag Q4_23_NHS_review was removed from gene: FBXW11.
Skeletal dysplasia v5.3 FBXW11 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 ERI1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ERI1.
Tag Q4_23_NHS_review was removed from gene: ERI1.
Skeletal dysplasia v5.3 AXIN1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: AXIN1.
Skeletal dysplasia v5.3 AXIN1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 SETD5 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SETD5.
Tag Q3_23_NHS_review was removed from gene: SETD5.
Skeletal dysplasia v5.3 SETD5 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 UBA2 Achchuthan Shanmugasundram reviewed gene: UBA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Skeletal dysplasia v5.3 TNFRSF11A Achchuthan Shanmugasundram reviewed gene: TNFRSF11A: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Skeletal dysplasia v5.3 SETD5 Achchuthan Shanmugasundram commented on gene: SETD5: The rating of this gene has been updated togreenand the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 PSMC3 Achchuthan Shanmugasundram commented on gene: PSMC3: The rating of this gene has been updated togreenand the mode of inheritance updated to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 FBXW11 Achchuthan Shanmugasundram reviewed gene: FBXW11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Skeletal dysplasia v5.3 ERI1 Achchuthan Shanmugasundram commented on gene: ERI1: The rating of this gene has been updated togreenand the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 AXIN1 Achchuthan Shanmugasundram commented on gene: AXIN1: The rating of this gene has been updated togreenand the mode of inheritance updated to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.
Skeletal dysplasia v5.3 ANAPC1 Achchuthan Shanmugasundram reviewed gene: ANAPC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Skeletal dysplasia v5.2 UBA2 Achchuthan Shanmugasundram Source NHS GMS was added to UBA2.
Source Expert Review Green was added to UBA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 TNFRSF11A Achchuthan Shanmugasundram Mode of inheritance for gene TNFRSF11A was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Skeletal dysplasia v5.2 SETD5 Achchuthan Shanmugasundram Source Expert Review Green was added to SETD5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 PSMC3 Achchuthan Shanmugasundram Source NHS GMS was added to PSMC3.
Source Expert Review Green was added to PSMC3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 FBXW11 Achchuthan Shanmugasundram Source NHS GMS was added to FBXW11.
Source Expert Review Green was added to FBXW11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 ERI1 Achchuthan Shanmugasundram Source Expert Review Green was added to ERI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 AXIN1 Achchuthan Shanmugasundram Source NHS GMS was added to AXIN1.
Source Expert Review Green was added to AXIN1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v5.2 ANAPC1 Achchuthan Shanmugasundram Source NHS GMS was added to ANAPC1.
Source Expert Review Green was added to ANAPC1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal ciliopathies v4.3 KIAA0586 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated togreenand the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Skeletal ciliopathies v4.3 KIAA0586 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KIAA0586.
Skeletal ciliopathies v4.3 PMM2 Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: PMM2.
Tag Q3_23_demote_red was removed from gene: PMM2.
Skeletal ciliopathies v4.3 PMM2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated to redfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to red following NHS Genomic Medicine Service approval.
Skeletal ciliopathies v4.3 PMM2 Achchuthan Shanmugasundram reviewed gene: PMM2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Skeletal ciliopathies v4.3 KIAA0586 Achchuthan Shanmugasundram reviewed gene: KIAA0586: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Skeletal ciliopathies v4.2 PMM2 Achchuthan Shanmugasundram Source Expert Review Red was added to PMM2.
Source NHS GMS was added to PMM2.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Skeletal ciliopathies v4.2 KIAA0586 Achchuthan Shanmugasundram Source Expert Review Green was added to KIAA0586.
Source NHS GMS was added to KIAA0586.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Limb disorders v5.4 FBXW11 Achchuthan Shanmugasundram Tag Q4_21_NHS_review was removed from gene: FBXW11.
Tag Q4_23_promote_green was removed from gene: FBXW11.
Limb disorders v5.4 FBXW11 Eleanor Williams edited their review of gene: FBXW11: Added comment: The rating of this gene has been updated togreenand the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown'following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Limb disorders v5.3 FBXW11 Achchuthan Shanmugasundram Source NHS GMS was added to FBXW11.
Source Expert Review Green was added to FBXW11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.3 SLC6A20 Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: SLC6A20.
Tag Q4_23_expert_review was removed from gene: SLC6A20.
Likely inborn error of metabolism v5.3 VPS33A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: VPS33A.
Likely inborn error of metabolism v5.3 VPS16 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: VPS16.
Likely inborn error of metabolism v5.3 SEC23B Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: SEC23B.
Likely inborn error of metabolism v5.3 PTCD3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PTCD3.
Likely inborn error of metabolism v5.3 PIGM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PIGM.
Tag Q4_23_NHS_review was removed from gene: PIGM.
Likely inborn error of metabolism v5.3 NUS1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NUS1.
Likely inborn error of metabolism v5.3 MRM2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MRM2.
Likely inborn error of metabolism v5.3 LMF1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: LMF1.
Likely inborn error of metabolism v5.3 HSPA9 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HSPA9.
Tag Q4_23_NHS_review was removed from gene: HSPA9.
Likely inborn error of metabolism v5.3 GRN Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GRN.
Likely inborn error of metabolism v5.3 GPIHBP1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GPIHBP1.
Likely inborn error of metabolism v5.3 EDEM3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: EDEM3.
Likely inborn error of metabolism v5.3 CTSF Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CTSF.
Likely inborn error of metabolism v5.3 COX5A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: COX5A.
Likely inborn error of metabolism v5.3 ATP5E Achchuthan Shanmugasundram Tag new-gene-name was removed from gene: ATP5E.
Tag Q4_23_promote_green was removed from gene: ATP5E.
Likely inborn error of metabolism v5.3 ACACA Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ACACA.
Tag Q4_23_NHS_review was removed from gene: ACACA.
Likely inborn error of metabolism v5.3 VPS33A Sarah Leigh commented on gene: VPS33A: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Likely inborn error of metabolism v5.3 VPS16 Sarah Leigh commented on gene: VPS16: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Likely inborn error of metabolism v5.3 SLC6A20 Sarah Leigh commented on gene: SLC6A20: The rating of this gene has been updated to red following NHS Genomic Medicine Service approval. Comment from GMS: 'Demotion of a green gene - disease association refuted in OMIM, as the single variant has been classified as common in gnomAD database.'
Likely inborn error of metabolism v5.3 SEC23B Sarah Leigh reviewed gene: SEC23B: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 PTCD3 Sarah Leigh edited their review of gene: PTCD3: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 PIGM Sarah Leigh edited their review of gene: PIGM: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 NUS1 Sarah Leigh reviewed gene: NUS1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Likely inborn error of metabolism v5.3 MRM2 Sarah Leigh edited their review of gene: MRM2: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 LMF1 Sarah Leigh commented on gene: LMF1: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Likely inborn error of metabolism v5.3 HSPA9 Sarah Leigh edited their review of gene: HSPA9: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 GRN Sarah Leigh edited their review of gene: GRN: Added comment: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 GPIHBP1 Sarah Leigh commented on gene: GPIHBP1: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Likely inborn error of metabolism v5.3 EDEM3 Sarah Leigh commented on gene: EDEM3: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Likely inborn error of metabolism v5.3 CTSF Sarah Leigh edited their review of gene: CTSF: Added comment: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 COX5A Sarah Leigh edited their review of gene: COX5A: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 ATP5E Sarah Leigh edited their review of gene: ATP5E: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.3 ACACA Sarah Leigh edited their review of gene: ACACA: Added comment: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.2 VPS33A Achchuthan Shanmugasundram Source Expert Review Green was added to VPS33A.
Source NHS GMS was added to VPS33A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 VPS16 Achchuthan Shanmugasundram Source Expert Review Green was added to VPS16.
Source NHS GMS was added to VPS16.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 SLC6A20 Achchuthan Shanmugasundram Source Expert Review Red was added to SLC6A20.
Source NHS GMS was added to SLC6A20.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Likely inborn error of metabolism v5.2 SEC23B Achchuthan Shanmugasundram Mode of inheritance for gene SEC23B was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v5.2 PTCD3 Achchuthan Shanmugasundram Source Expert Review Green was added to PTCD3.
Source NHS GMS was added to PTCD3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 PIGM Achchuthan Shanmugasundram Source Expert Review Green was added to PIGM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 NUS1 Achchuthan Shanmugasundram Source Expert Review Green was added to NUS1.
Source NHS GMS was added to NUS1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 MRM2 Achchuthan Shanmugasundram Source Expert Review Green was added to MRM2.
Source NHS GMS was added to MRM2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 LMF1 Achchuthan Shanmugasundram Source Expert Review Green was added to LMF1.
Source NHS GMS was added to LMF1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 HSPA9 Achchuthan Shanmugasundram Source Expert Review Green was added to HSPA9.
Source NHS GMS was added to HSPA9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 GRN Achchuthan Shanmugasundram Source Expert Review Green was added to GRN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 GPIHBP1 Achchuthan Shanmugasundram Source Expert Review Green was added to GPIHBP1.
Source NHS GMS was added to GPIHBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 EDEM3 Achchuthan Shanmugasundram Source Expert Review Green was added to EDEM3.
Source NHS GMS was added to EDEM3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 CTSF Achchuthan Shanmugasundram Source Expert Review Green was added to CTSF.
Source NHS GMS was added to CTSF.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 COX5A Achchuthan Shanmugasundram Source Expert Review Green was added to COX5A.
Source NHS GMS was added to COX5A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 ATP5E Achchuthan Shanmugasundram Source Expert Review Green was added to ATP5E.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism v5.2 ACACA Achchuthan Shanmugasundram Source Expert Review Green was added to ACACA.
Source NHS GMS was added to ACACA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital disorders of glycosylation v5.3 SEC23B Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: SEC23B.
Congenital disorders of glycosylation v5.3 PIGM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PIGM.
Congenital disorders of glycosylation v5.3 SEC23B Sarah Leigh edited their review of gene: SEC23B: Added comment: The mode of inheritance of this gene has been updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital disorders of glycosylation v5.3 PIGM Sarah Leigh edited their review of gene: PIGM: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital disorders of glycosylation v5.2 SEC23B Achchuthan Shanmugasundram Source NHS GMS was added to SEC23B.
Mode of inheritance for gene SEC23B was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Congenital disorders of glycosylation v5.2 PIGM Achchuthan Shanmugasundram Source Expert Review Green was added to PIGM.
Source NHS GMS was added to PIGM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SPI1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SPI1.
Tag Q4_23_NHS_review was removed from gene: SPI1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 TRAF3IP2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TRAF3IP2.
Tag Q4_23_NHS_review was removed from gene: TRAF3IP2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 TFRC Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TFRC.
Tag Q4_23_NHS_review was removed from gene: TFRC.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 STAT6 Achchuthan Shanmugasundram Tag watchlist was removed from gene: STAT6.
Tag Q4_23_promote_green was removed from gene: STAT6.
Tag treatable tag was added to gene: STAT6.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SEC61A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SEC61A1.
Tag Q4_23_NHS_review was removed from gene: SEC61A1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SAMD9L Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SAMD9L.
Tag Q4_23_NHS_review was removed from gene: SAMD9L.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 RELA Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RELA.
Tag Q4_23_NHS_review was removed from gene: RELA.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 REL Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: REL.
Tag Q4_23_NHS_review was removed from gene: REL.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 RANBP2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RANBP2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 PTPN2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PTPN2.
Tag Q4_23_NHS_review was removed from gene: PTPN2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 PSMB10 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PSMB10.
Tag Q4_23_NHS_review was removed from gene: PSMB10.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 POLD1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: POLD1.
Tag Q4_23_NHS_review was removed from gene: POLD1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 NLRP1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NLRP1.
Tag Q4_23_NHS_review was removed from gene: NLRP1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 NFAT5 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NFAT5.
Tag Q4_23_NHS_review was removed from gene: NFAT5.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 MECOM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MECOM.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 MCTS1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MCTS1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 LYN Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: LYN.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 JAK1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: JAK1.
Tag Q4_23_NHS_review was removed from gene: JAK1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IRF4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IRF4.
Tag Q4_23_NHS_review was removed from gene: IRF4.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IRF2BP2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IRF2BP2.
Tag Q4_23_NHS_review was removed from gene: IRF2BP2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IL23R Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IL23R.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 HYOU1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HYOU1.
Tag Q4_23_NHS_review was removed from gene: HYOU1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 HMOX1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HMOX1.
Tag Q4_23_NHS_review was removed from gene: HMOX1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DUT Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: DUT.
Tag Q4_23_NHS_review was removed from gene: DUT.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CXCR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CXCR2.
Tag Q4_23_NHS_review was removed from gene: CXCR2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CR2.
Tag Q4_23_NHS_review was removed from gene: CR2.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CD81 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CD81.
Tag Q4_23_NHS_review was removed from gene: CD81.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CD4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CD4.
Tag Q4_23_NHS_review was removed from gene: CD4.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CBLB Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CBLB.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 AICDA Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: AICDA.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 OTULIN Achchuthan Shanmugasundram Tag Q3_23_MOI was removed from gene: OTULIN.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DOCK11 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DOCK11.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DIAPH1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DIAPH1.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 ARPC5 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ARPC5.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DCLRE1B Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: DCLRE1B.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 STAT5B Achchuthan Shanmugasundram Tag for-review was removed from gene: STAT5B.
Tag to_be_confirmed_NHSE was removed from gene: STAT5B.
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 TRAF3IP2 Sarah Leigh reviewed gene: TRAF3IP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 TFRC Sarah Leigh reviewed gene: TFRC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 STAT6 Sarah Leigh reviewed gene: STAT6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 STAT5B Sarah Leigh reviewed gene: STAT5B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SPI1 Sarah Leigh reviewed gene: SPI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SEC61A1 Sarah Leigh reviewed gene: SEC61A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 SAMD9L Sarah Leigh reviewed gene: SAMD9L: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 RELA Sarah Leigh reviewed gene: RELA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 REL Sarah Leigh reviewed gene: REL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 RANBP2 Sarah Leigh reviewed gene: RANBP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 PTPN2 Sarah Leigh reviewed gene: PTPN2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 PSMB10 Sarah Leigh edited their review of gene: PSMB10: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 POLD1 Sarah Leigh reviewed gene: POLD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 OTULIN Sarah Leigh edited their review of gene: OTULIN: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 NLRP1 Sarah Leigh reviewed gene: NLRP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 NFAT5 Sarah Leigh edited their review of gene: NFAT5: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 MECOM Sarah Leigh reviewed gene: MECOM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 MCTS1 Sarah Leigh reviewed gene: MCTS1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 LYN Sarah Leigh reviewed gene: LYN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 JAK1 Sarah Leigh reviewed gene: JAK1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IRF4 Sarah Leigh reviewed gene: IRF4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IRF2BP2 Sarah Leigh reviewed gene: IRF2BP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 IL23R Sarah Leigh reviewed gene: IL23R: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 HYOU1 Sarah Leigh reviewed gene: HYOU1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 HMOX1 Sarah Leigh reviewed gene: HMOX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DUT Sarah Leigh reviewed gene: DUT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DOCK11 Sarah Leigh reviewed gene: DOCK11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DIAPH1 Sarah Leigh reviewed gene: DIAPH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 DCLRE1B Sarah Leigh reviewed gene: DCLRE1B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CXCR2 Sarah Leigh reviewed gene: CXCR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CR2 Sarah Leigh edited their review of gene: CR2: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CD81 Sarah Leigh reviewed gene: CD81: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CD4 Sarah Leigh reviewed gene: CD4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 CBLB Sarah Leigh reviewed gene: CBLB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 ARPC5 Sarah Leigh reviewed gene: ARPC5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.3 AICDA Sarah Leigh reviewed gene: AICDA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 TRAF3IP2 Achchuthan Shanmugasundram Source NHS GMS was added to TRAF3IP2.
Source Expert Review Green was added to TRAF3IP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 TFRC Achchuthan Shanmugasundram Source NHS GMS was added to TFRC.
Source Expert Review Green was added to TFRC.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 STAT6 Achchuthan Shanmugasundram Source NHS GMS was added to STAT6.
Source Expert Review Green was added to STAT6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 STAT5B Achchuthan Shanmugasundram Mode of inheritance for gene STAT5B was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 SPI1 Achchuthan Shanmugasundram Source NHS GMS was added to SPI1.
Source Expert Review Green was added to SPI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 SEC61A1 Achchuthan Shanmugasundram Source NHS GMS was added to SEC61A1.
Source Expert Review Green was added to SEC61A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 SAMD9L Achchuthan Shanmugasundram Source Expert Review Green was added to SAMD9L.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 RELA Achchuthan Shanmugasundram Source NHS GMS was added to RELA.
Source Expert Review Green was added to RELA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 REL Achchuthan Shanmugasundram Source NHS GMS was added to REL.
Source Expert Review Green was added to REL.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 RANBP2 Achchuthan Shanmugasundram Source Expert Review Green was added to RANBP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 PTPN2 Achchuthan Shanmugasundram Source NHS GMS was added to PTPN2.
Source Expert Review Green was added to PTPN2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 PSMB10 Achchuthan Shanmugasundram Source NHS GMS was added to PSMB10.
Source Expert Review Green was added to PSMB10.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 POLD1 Achchuthan Shanmugasundram Source NHS GMS was added to POLD1.
Source Expert Review Green was added to POLD1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 OTULIN Achchuthan Shanmugasundram Mode of inheritance for gene OTULIN was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 NLRP1 Achchuthan Shanmugasundram Source Expert Review Green was added to NLRP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 NFAT5 Achchuthan Shanmugasundram Source NHS GMS was added to NFAT5.
Source Expert Review Green was added to NFAT5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 MECOM Achchuthan Shanmugasundram Source NHS GMS was added to MECOM.
Source Expert Review Green was added to MECOM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 MCTS1 Achchuthan Shanmugasundram Source NHS GMS was added to MCTS1.
Source Expert Review Green was added to MCTS1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 LYN Achchuthan Shanmugasundram Source NHS GMS was added to LYN.
Source Expert Review Green was added to LYN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 JAK1 Achchuthan Shanmugasundram Source NHS GMS was added to JAK1.
Source Expert Review Green was added to JAK1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 IRF4 Achchuthan Shanmugasundram Source NHS GMS was added to IRF4.
Source Expert Review Green was added to IRF4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 IRF2BP2 Achchuthan Shanmugasundram Source NHS GMS was added to IRF2BP2.
Source Expert Review Green was added to IRF2BP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 IL23R Achchuthan Shanmugasundram Source NHS GMS was added to IL23R.
Source Expert Review Green was added to IL23R.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 HYOU1 Achchuthan Shanmugasundram Source NHS GMS was added to HYOU1.
Source Expert Review Green was added to HYOU1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 HMOX1 Achchuthan Shanmugasundram Source NHS GMS was added to HMOX1.
Source Expert Review Green was added to HMOX1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 DUT Achchuthan Shanmugasundram Source NHS GMS was added to DUT.
Source Expert Review Green was added to DUT.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 DOCK11 Achchuthan Shanmugasundram Source NHS GMS was added to DOCK11.
Source Expert Review Green was added to DOCK11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 DIAPH1 Achchuthan Shanmugasundram Source NHS GMS was added to DIAPH1.
Source Expert Review Green was added to DIAPH1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 DCLRE1B Achchuthan Shanmugasundram Source Expert Review Amber was added to DCLRE1B.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 CXCR2 Achchuthan Shanmugasundram Source NHS GMS was added to CXCR2.
Source Expert Review Green was added to CXCR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 CR2 Achchuthan Shanmugasundram Source NHS GMS was added to CR2.
Source Expert Review Green was added to CR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 CD81 Achchuthan Shanmugasundram Source NHS GMS was added to CD81.
Source Expert Review Green was added to CD81.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 CD4 Achchuthan Shanmugasundram Source NHS GMS was added to CD4.
Source Expert Review Green was added to CD4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 CBLB Achchuthan Shanmugasundram Source NHS GMS was added to CBLB.
Source Expert Review Green was added to CBLB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 ARPC5 Achchuthan Shanmugasundram Source NHS GMS was added to ARPC5.
Source Expert Review Green was added to ARPC5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v5.2 AICDA Achchuthan Shanmugasundram Mode of inheritance for gene AICDA was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Thalassaemia and other haemoglobinopathies v1.9 HBG2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBG2.
Thalassaemia and other haemoglobinopathies v1.9 HBG1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBG1.
Thalassaemia and other haemoglobinopathies v1.9 HBA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBA2.
Thalassaemia and other haemoglobinopathies v1.9 HBG2 Sarah Leigh reviewed gene: HBG2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Thalassaemia and other haemoglobinopathies v1.9 HBG1 Sarah Leigh reviewed gene: HBG1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Thalassaemia and other haemoglobinopathies v1.9 HBA2 Sarah Leigh reviewed gene: HBA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Thalassaemia and other haemoglobinopathies v1.8 HBG2 Achchuthan Shanmugasundram Source Expert Review Green was added to HBG2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Thalassaemia and other haemoglobinopathies v1.8 HBG1 Achchuthan Shanmugasundram Source Expert Review Green was added to HBG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Thalassaemia and other haemoglobinopathies v1.8 HBA2 Achchuthan Shanmugasundram Source Expert Review Green was added to HBA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Haemoglobinopathy trait or carrier testing v1.9 HBG2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBG2.
Haemoglobinopathy trait or carrier testing v1.9 HBG1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBG1.
Haemoglobinopathy trait or carrier testing v1.9 HBA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBA2.
Haemoglobinopathy trait or carrier testing v1.9 HBG2 Sarah Leigh reviewed gene: HBG2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Haemoglobinopathy trait or carrier testing v1.9 HBG1 Sarah Leigh reviewed gene: HBG1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Haemoglobinopathy trait or carrier testing v1.9 HBA2 Sarah Leigh reviewed gene: HBA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Haemoglobinopathy trait or carrier testing v1.8 HBG2 Achchuthan Shanmugasundram Source Expert Review Green was added to HBG2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Haemoglobinopathy trait or carrier testing v1.8 HBG1 Achchuthan Shanmugasundram Source Expert Review Green was added to HBG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Haemoglobinopathy trait or carrier testing v1.8 HBA2 Achchuthan Shanmugasundram Source Expert Review Green was added to HBA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Neonatal diabetes v4.6 ONECUT1 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: ONECUT1.
Neonatal diabetes v4.6 CNOT1 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: CNOT1.
Neonatal diabetes v4.6 ONECUT1 Sarah Leigh reviewed gene: ONECUT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Neonatal diabetes v4.6 CNOT1 Sarah Leigh reviewed gene: CNOT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Neonatal diabetes v4.5 ONECUT1 Achchuthan Shanmugasundram Source NHS GMS was added to ONECUT1.
Source Expert Review Green was added to ONECUT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Neonatal diabetes v4.5 CNOT1 Achchuthan Shanmugasundram Source NHS GMS was added to CNOT1.
Source Expert Review Green was added to CNOT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.52 AKT2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: AKT2.
Tag Q3_23_NHS_review was removed from gene: AKT2.
Severe insulin resistance and lipodystrophy syndromes v4.52 WRN Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 WRN Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: WRN.
Tag Q3_23_NHS_review was removed from gene: WRN.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB8 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PSMB8.
Tag Q3_23_NHS_review was removed from gene: PSMB8.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB8 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB4 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB4 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PSMB4.
Tag Q3_23_NHS_review was removed from gene: PSMB4.
Severe insulin resistance and lipodystrophy syndromes v4.52 POC1A Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: POC1A.
Tag Q3_23_NHS_review was removed from gene: POC1A.
Severe insulin resistance and lipodystrophy syndromes v4.52 POC1A Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PIK3R1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toMONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PIK3R1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PIK3R1.
Tag Q3_23_NHS_review was removed from gene: PIK3R1.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCYT1A Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCYT1A Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PCYT1A.
Tag Q3_23_NHS_review was removed from gene: PCYT1A.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCNT Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PCNT.
Tag Q3_23_NHS_review was removed from gene: PCNT.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCNT Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 MFN2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: MFN2.
Tag Q3_23_NHS_review was removed from gene: MFN2.
Severe insulin resistance and lipodystrophy syndromes v4.52 MFN2 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 EPHX1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toMONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 EPHX1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: EPHX1.
Tag Q3_23_NHS_review was removed from gene: EPHX1.
Severe insulin resistance and lipodystrophy syndromes v4.52 BLM Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: BLM.
Tag Q3_23_NHS_review was removed from gene: BLM.
Severe insulin resistance and lipodystrophy syndromes v4.52 BLM Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 ALMS1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ALMS1.
Tag Q3_23_NHS_review was removed from gene: ALMS1.
Severe insulin resistance and lipodystrophy syndromes v4.52 ALMS1 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 WRN Achchuthan Shanmugasundram commented on gene: WRN: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB8 Achchuthan Shanmugasundram commented on gene: PSMB8: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PSMB4 Achchuthan Shanmugasundram commented on gene: PSMB4: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 POC1A Achchuthan Shanmugasundram commented on gene: POC1A: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PIK3R1 Achchuthan Shanmugasundram commented on gene: PIK3R1: The rating of this gene has been updated toGreenand the mode of inheritance set toMONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCYT1A Achchuthan Shanmugasundram commented on gene: PCYT1A: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 PCNT Achchuthan Shanmugasundram commented on gene: PCNT: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 MFN2 Achchuthan Shanmugasundram commented on gene: MFN2: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 EPHX1 Achchuthan Shanmugasundram commented on gene: EPHX1: The rating of this gene has been updated toGreenand the mode of inheritance set toMONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 BLM Achchuthan Shanmugasundram commented on gene: BLM: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 ALMS1 Achchuthan Shanmugasundram commented on gene: ALMS1: The rating of this gene has been updated toGreenand the mode of inheritance set toBIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Severe insulin resistance and lipodystrophy syndromes v4.52 AKT2 Achchuthan Shanmugasundram edited their review of gene: AKT2: Added comment: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remains amber. Comment from GMS: 'Should be amber. Another family is needed for AKT2 for this to be upgraded to Green. The two variants used as evidence, p.Arg467Trp and p.Arg208Lys, far too common in gnomAD to be causing a rare AD disorder.'; Changed rating: AMBER
Severe insulin resistance and lipodystrophy syndromes v4.51 WRN Achchuthan Shanmugasundram Source Expert Review Green was added to WRN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 PSMB8 Achchuthan Shanmugasundram Source Expert Review Green was added to PSMB8.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 PSMB4 Achchuthan Shanmugasundram Source Expert Review Green was added to PSMB4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 POC1A Achchuthan Shanmugasundram Source Expert Review Green was added to POC1A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 PIK3R1 Achchuthan Shanmugasundram Source Expert Review Green was added to PIK3R1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 PCYT1A Achchuthan Shanmugasundram Source Expert Review Green was added to PCYT1A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 PCNT Achchuthan Shanmugasundram Source Expert Review Green was added to PCNT.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 MFN2 Achchuthan Shanmugasundram Source Expert Review Green was added to MFN2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 EPHX1 Achchuthan Shanmugasundram Source Expert Review Green was added to EPHX1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 BLM Achchuthan Shanmugasundram Source Expert Review Green was added to BLM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe insulin resistance and lipodystrophy syndromes v4.51 ALMS1 Achchuthan Shanmugasundram Source Expert Review Green was added to ALMS1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric disorders - additional genes v4.3 NOTCH3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NOTCH3.
Tag Q4_23_expert_review was removed from gene: NOTCH3.
Paediatric disorders - additional genes v4.3 TAB2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TAB2.
Paediatric disorders - additional genes v4.3 TAB2 Sarah Leigh edited their review of gene: TAB2: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Paediatric disorders - additional genes v4.3 NOTCH3 Sarah Leigh reviewed gene: NOTCH3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Paediatric disorders - additional genes v4.2 TAB2 Achchuthan Shanmugasundram Source Expert Review Green was added to TAB2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric disorders - additional genes v4.2 NOTCH3 Achchuthan Shanmugasundram Source Expert Review Green was added to NOTCH3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.11 FAM111A Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: FAM111A.
Tag Q4_23_NHS_review was removed from gene: FAM111A.
Tag Q4_23_expert_review was removed from gene: FAM111A.
Intellectual disability v6.11 DPP6 Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: DPP6.
Tag Q4_23_NHS_review was removed from gene: DPP6.
Tag Q4_23_expert_review was removed from gene: DPP6.
Intellectual disability v6.11 ZBTB47 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ZBTB47.
Intellectual disability v6.11 VCP Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: VCP.
Intellectual disability v6.11 TEFM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TEFM.
Intellectual disability v6.11 SRSF1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SRSF1.
Intellectual disability v6.11 SHQ1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SHQ1.
Intellectual disability v6.11 RPL10 Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: RPL10.
Intellectual disability v6.11 RELN Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: RELN.
Intellectual disability v6.11 RBL2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RBL2.
Tag Q4_23_NHS_review was removed from gene: RBL2.
Intellectual disability v6.11 RAP1B Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RAP1B.
Intellectual disability v6.11 MYH10 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MYH10.
Intellectual disability v6.11 MAST4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MAST4.
Intellectual disability v6.11 KMT2B Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KMT2B.
Intellectual disability v6.11 ERI1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ERI1.
Intellectual disability v6.11 COX11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: COX11.
Intellectual disability v6.11 CLDN11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLDN11.
Intellectual disability v6.11 CLCN6 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLCN6.
Intellectual disability v6.11 CDK16 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CDK16.
Tag Q4_23_NHS_review was removed from gene: CDK16.
Intellectual disability v6.11 CASP2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CASP2.
Intellectual disability v6.11 ARF3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ARF3.
Intellectual disability v6.11 ACACA Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ACACA.
Intellectual disability v6.11 FAR1 Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: FAR1.
Intellectual disability v6.11 U2AF2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: U2AF2.
Tag Q3_23_NHS_review was removed from gene: U2AF2.
Intellectual disability v6.11 TTI1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TTI1.
Intellectual disability v6.11 TSPOAP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TSPOAP1.
Intellectual disability v6.11 TMEM63B Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TMEM63B.
Intellectual disability v6.11 SLC30A9 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC30A9.
Intellectual disability v6.11 RPS6KA3 Achchuthan Shanmugasundram Tag Q3_23_MOI was removed from gene: RPS6KA3.
Intellectual disability v6.11 RAB5C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: RAB5C.
Intellectual disability v6.11 PSMC3 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PSMC3.
Intellectual disability v6.11 PPP1R3F Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PPP1R3F.
Intellectual disability v6.11 PIP5K1C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PIP5K1C.
Intellectual disability v6.11 PABPC1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PABPC1.
Tag Q3_23_MOI was removed from gene: PABPC1.
Tag Q3_23_phenotype was removed from gene: PABPC1.
Intellectual disability v6.11 NR2F2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: NR2F2.
Tag Q3_23_NHS_review was removed from gene: NR2F2.
Intellectual disability v6.11 NEUROG1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: NEUROG1.
Tag Q3_23_NHS_review was removed from gene: NEUROG1.
Intellectual disability v6.11 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Intellectual disability v6.11 KCNH5 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: KCNH5.
Intellectual disability v6.11 ESAM Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ESAM.
Tag Q3_23_NHS_review was removed from gene: ESAM.
Intellectual disability v6.11 EIF4A2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: EIF4A2.
Intellectual disability v6.11 DHX9 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DHX9.
Intellectual disability v6.11 DAGLA Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DAGLA.
Intellectual disability v6.11 CNOT9 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CNOT9.
Intellectual disability v6.11 ATP6V0C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ATP6V0C.
Tag Q3_23_NHS_review was removed from gene: ATP6V0C.
Intellectual disability v6.11 AGTPBP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: AGTPBP1.
Intellectual disability v6.11 ZBTB47 Sarah Leigh edited their review of gene: ZBTB47: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 VCP Sarah Leigh reviewed gene: VCP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 U2AF2 Sarah Leigh reviewed gene: U2AF2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 TTI1 Sarah Leigh commented on gene: TTI1: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 TSPOAP1 Sarah Leigh edited their review of gene: TSPOAP1: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 TMEM63B Sarah Leigh reviewed gene: TMEM63B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 TEFM Sarah Leigh reviewed gene: TEFM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 SRSF1 Sarah Leigh reviewed gene: SRSF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 SLC30A9 Sarah Leigh edited their review of gene: SLC30A9: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Intellectual disability v6.11 SHQ1 Sarah Leigh edited their review of gene: SHQ1: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 RPS6KA3 Sarah Leigh reviewed gene: RPS6KA3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability v6.11 RPL10 Sarah Leigh commented on gene: RPL10: The mode of inheritance of this gene has been updated to X-LINKED: hemizygous mutation in males, biallelic mutations in females following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 RELN Sarah Leigh reviewed gene: RELN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability v6.11 RBL2 Sarah Leigh commented on gene: RBL2: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 RAP1B Sarah Leigh reviewed gene: RAP1B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 RAB5C Sarah Leigh reviewed gene: RAB5C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 PSMC3 Sarah Leigh reviewed gene: PSMC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 PPP1R3F Sarah Leigh reviewed gene: PPP1R3F: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability v6.11 PIP5K1C Sarah Leigh reviewed gene: PIP5K1C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 PABPC1 Sarah Leigh edited their review of gene: PABPC1: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability v6.11 NR2F2 Sarah Leigh reviewed gene: NR2F2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 NEUROG1 Sarah Leigh reviewed gene: NEUROG1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 MYH10 Sarah Leigh reviewed gene: MYH10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 MAST4 Sarah Leigh edited their review of gene: MAST4: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 LETM1 Sarah Leigh commented on gene: LETM1: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 KMT2B Sarah Leigh reviewed gene: KMT2B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Intellectual disability v6.11 KCNH5 Sarah Leigh reviewed gene: KCNH5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 FAR1 Sarah Leigh commented on gene: FAR1: The mode of inheritance of this gene has been updated to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 FAM111A Sarah Leigh commented on gene: FAM111A: The rating of this gene has been updated to red following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 ESAM Sarah Leigh reviewed gene: ESAM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 ERI1 Sarah Leigh reviewed gene: ERI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 EIF4A2 Sarah Leigh commented on gene: EIF4A2: The rating of this gene has been updated to Green and the mode of inheritance set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval
Intellectual disability v6.11 DPP6 Sarah Leigh reviewed gene: DPP6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Intellectual disability v6.11 DHX9 Sarah Leigh reviewed gene: DHX9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 DAGLA Sarah Leigh reviewed gene: DAGLA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 COX11 Sarah Leigh edited their review of gene: COX11: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 CNOT9 Sarah Leigh reviewed gene: CNOT9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 CLDN11 Sarah Leigh reviewed gene: CLDN11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 CLCN6 Sarah Leigh commented on gene: CLCN6: The rating of this gene has been updated to Green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 CDK16 Sarah Leigh commented on gene: CDK16: The rating of this gene has been updated to green and the mode of inheritance updated to X-LINKED: hemizygous mutation in males, biallelic mutations in females following NHS Genomic Medicine Service approval.
Intellectual disability v6.11 CASP2 Sarah Leigh edited their review of gene: CASP2: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Intellectual disability v6.11 ATP6V0C Sarah Leigh reviewed gene: ATP6V0C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v6.11 ARF3 Sarah Leigh reviewed gene: ARF3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Intellectual disability v6.11 AGTPBP1 Sarah Leigh reviewed gene: AGTPBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.11 ACACA Sarah Leigh edited their review of gene: ACACA: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v6.10 ZBTB47 Achchuthan Shanmugasundram Source Expert Review Green was added to ZBTB47.
Source NHS GMS was added to ZBTB47.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 VCP Achchuthan Shanmugasundram Source Expert Review Green was added to VCP.
Source NHS GMS was added to VCP.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 U2AF2 Achchuthan Shanmugasundram Source Expert Review Green was added to U2AF2.
Source NHS GMS was added to U2AF2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 TTI1 Achchuthan Shanmugasundram Source Expert Review Green was added to TTI1.
Source NHS GMS was added to TTI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 TSPOAP1 Achchuthan Shanmugasundram Source Expert Review Green was added to TSPOAP1.
Source NHS GMS was added to TSPOAP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 TMEM63B Achchuthan Shanmugasundram Source Expert Review Green was added to TMEM63B.
Source NHS GMS was added to TMEM63B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 TEFM Achchuthan Shanmugasundram Source Expert Review Green was added to TEFM.
Source NHS GMS was added to TEFM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 SRSF1 Achchuthan Shanmugasundram Source Expert Review Green was added to SRSF1.
Source NHS GMS was added to SRSF1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 SLC30A9 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC30A9.
Source NHS GMS was added to SLC30A9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 SHQ1 Achchuthan Shanmugasundram Source Expert Review Green was added to SHQ1.
Source NHS GMS was added to SHQ1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 RPS6KA3 Achchuthan Shanmugasundram Source NHS GMS was added to RPS6KA3.
Mode of inheritance for gene RPS6KA3 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability v6.10 RPL10 Achchuthan Shanmugasundram Source NHS GMS was added to RPL10.
Mode of inheritance for gene RPL10 was changed from X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability v6.10 RELN Achchuthan Shanmugasundram Source NHS GMS was added to RELN.
Mode of inheritance for gene RELN was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability v6.10 RBL2 Achchuthan Shanmugasundram Source Expert Review Green was added to RBL2.
Source NHS GMS was added to RBL2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 RAP1B Achchuthan Shanmugasundram Source Expert Review Green was added to RAP1B.
Source NHS GMS was added to RAP1B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 RAB5C Achchuthan Shanmugasundram Source Expert Review Green was added to RAB5C.
Source NHS GMS was added to RAB5C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 PSMC3 Achchuthan Shanmugasundram Source Expert Review Green was added to PSMC3.
Source NHS GMS was added to PSMC3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 PPP1R3F Achchuthan Shanmugasundram Source Expert Review Green was added to PPP1R3F.
Source NHS GMS was added to PPP1R3F.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 PIP5K1C Achchuthan Shanmugasundram Source Expert Review Green was added to PIP5K1C.
Source NHS GMS was added to PIP5K1C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 PABPC1 Achchuthan Shanmugasundram Source Expert Review Green was added to PABPC1.
Source NHS GMS was added to PABPC1.
Mode of inheritance for gene PABPC1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 NR2F2 Achchuthan Shanmugasundram Source Expert Review Green was added to NR2F2.
Source NHS GMS was added to NR2F2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 NEUROG1 Achchuthan Shanmugasundram Source Expert Review Green was added to NEUROG1.
Source NHS GMS was added to NEUROG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 MYH10 Achchuthan Shanmugasundram Source Expert Review Green was added to MYH10.
Source NHS GMS was added to MYH10.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 MAST4 Achchuthan Shanmugasundram Source Expert Review Green was added to MAST4.
Source NHS GMS was added to MAST4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 LETM1 Achchuthan Shanmugasundram Source Expert Review Green was added to LETM1.
Source NHS GMS was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 KMT2B Achchuthan Shanmugasundram Source Expert Review Green was added to KMT2B.
Source NHS GMS was added to KMT2B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 KCNH5 Achchuthan Shanmugasundram Source Expert Review Green was added to KCNH5.
Source NHS GMS was added to KCNH5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 FAR1 Achchuthan Shanmugasundram Source NHS GMS was added to FAR1.
Mode of inheritance for gene FAR1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Intellectual disability v6.10 FAM111A Achchuthan Shanmugasundram Source Expert Review Red was added to FAM111A.
Source NHS GMS was added to FAM111A.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Intellectual disability v6.10 ESAM Achchuthan Shanmugasundram Source Expert Review Green was added to ESAM.
Source NHS GMS was added to ESAM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 ERI1 Achchuthan Shanmugasundram Source Expert Review Green was added to ERI1.
Source NHS GMS was added to ERI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 EIF4A2 Achchuthan Shanmugasundram Source Expert Review Green was added to EIF4A2.
Source NHS GMS was added to EIF4A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 DPP6 Achchuthan Shanmugasundram Source Expert Review Red was added to DPP6.
Source NHS GMS was added to DPP6.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Intellectual disability v6.10 DHX9 Achchuthan Shanmugasundram Source Expert Review Green was added to DHX9.
Source NHS GMS was added to DHX9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 DAGLA Achchuthan Shanmugasundram Source Expert Review Green was added to DAGLA.
Source NHS GMS was added to DAGLA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 COX11 Achchuthan Shanmugasundram Source Expert Review Green was added to COX11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 CNOT9 Achchuthan Shanmugasundram Source Expert Review Green was added to CNOT9.
Source NHS GMS was added to CNOT9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 CLDN11 Achchuthan Shanmugasundram Source Expert Review Green was added to CLDN11.
Source NHS GMS was added to CLDN11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 CLCN6 Achchuthan Shanmugasundram Source Expert Review Green was added to CLCN6.
Source NHS GMS was added to CLCN6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 CDK16 Achchuthan Shanmugasundram Source Expert Review Green was added to CDK16.
Source NHS GMS was added to CDK16.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 CASP2 Achchuthan Shanmugasundram Source Expert Review Green was added to CASP2.
Source NHS GMS was added to CASP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 ATP6V0C Achchuthan Shanmugasundram Source Expert Review Green was added to ATP6V0C.
Source NHS GMS was added to ATP6V0C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 ARF3 Achchuthan Shanmugasundram Source Expert Review Green was added to ARF3.
Source NHS GMS was added to ARF3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 AGTPBP1 Achchuthan Shanmugasundram Source Expert Review Green was added to AGTPBP1.
Source NHS GMS was added to AGTPBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.10 ACACA Achchuthan Shanmugasundram Source Expert Review Green was added to ACACA.
Source NHS GMS was added to ACACA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Inherited polyposis and early onset colorectal cancer - germline testing v2.11 GREM1 Achchuthan Shanmugasundram reviewed gene: GREM1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Inherited polyposis and early onset colorectal cancer - germline testing v2.11 GREM1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GREM1.
Tag Q4_23_NHS_review was removed from gene: GREM1.
Inherited polyposis and early onset colorectal cancer - germline testing v2.11 GREM1 Achchuthan Shanmugasundram Source Expert Review Green was added to GREM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric or syndromic cardiomyopathy v4.3 SLC22A5 Achchuthan Shanmugasundram Tag Q4_23_MOI was removed from gene: SLC22A5.
Paediatric or syndromic cardiomyopathy v4.3 TAB2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TAB2.
Paediatric or syndromic cardiomyopathy v4.3 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Paediatric or syndromic cardiomyopathy v4.3 LDB3 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LDB3.
Paediatric or syndromic cardiomyopathy v4.3 ELAC2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ELAC2.
Tag Q3_23_NHS_review was removed from gene: ELAC2.
Paediatric or syndromic cardiomyopathy v4.3 CAP2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CAP2.
Paediatric or syndromic cardiomyopathy v4.3 TAB2 Sarah Leigh edited their review of gene: TAB2: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Paediatric or syndromic cardiomyopathy v4.3 SLC22A5 Sarah Leigh commented on gene: SLC22A5: The mode of inheritance of this gene has been updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Paediatric or syndromic cardiomyopathy v4.3 LETM1 Sarah Leigh commented on gene: LETM1: The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Paediatric or syndromic cardiomyopathy v4.3 LDB3 Sarah Leigh reviewed gene: LDB3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paediatric or syndromic cardiomyopathy v4.3 ELAC2 Sarah Leigh reviewed gene: ELAC2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paediatric or syndromic cardiomyopathy v4.3 CAP2 Sarah Leigh reviewed gene: CAP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Paediatric or syndromic cardiomyopathy v4.2 TAB2 Achchuthan Shanmugasundram Source Expert Review Green was added to TAB2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric or syndromic cardiomyopathy v4.2 SLC22A5 Achchuthan Shanmugasundram Mode of inheritance for gene SLC22A5 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Paediatric or syndromic cardiomyopathy v4.2 LETM1 Achchuthan Shanmugasundram Source NHS GMS was added to LETM1.
Source Expert Review Green was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric or syndromic cardiomyopathy v4.2 LDB3 Achchuthan Shanmugasundram Source Expert Review Green was added to LDB3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric or syndromic cardiomyopathy v4.2 ELAC2 Achchuthan Shanmugasundram Source NHS GMS was added to ELAC2.
Source Expert Review Green was added to ELAC2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Paediatric or syndromic cardiomyopathy v4.2 CAP2 Achchuthan Shanmugasundram Source NHS GMS was added to CAP2.
Source Expert Review Green was added to CAP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cystic kidney disease v5.3 NEK8 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NEK8.
Cystic kidney disease v5.3 SEC63 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SEC63.
Tag Q3_23_NHS_review was removed from gene: SEC63.
Cystic kidney disease v5.3 PRKCSH Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PRKCSH.
Tag Q3_23_NHS_review was removed from gene: PRKCSH.
Cystic kidney disease v5.3 SEC63 Arina Puzriakova reviewed gene: SEC63: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cystic kidney disease v5.3 PRKCSH Arina Puzriakova reviewed gene: PRKCSH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cystic kidney disease v5.3 NEK8 Arina Puzriakova reviewed gene: NEK8: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cystic kidney disease v5.2 SEC63 Achchuthan Shanmugasundram Source Expert Review Green was added to SEC63.
Source NHS GMS was added to SEC63.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cystic kidney disease v5.2 PRKCSH Achchuthan Shanmugasundram Source Expert Review Green was added to PRKCSH.
Source NHS GMS was added to PRKCSH.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cystic kidney disease v5.2 NEK8 Achchuthan Shanmugasundram Source Expert Review Green was added to NEK8.
Source NHS GMS was added to NEK8.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.229 ZC4H2 Achchuthan Shanmugasundram Tag Q2_23_promote_green was removed from gene: ZC4H2.
Tag Q2_23_NHS_review was removed from gene: ZC4H2.
Congenital muscular dystrophy and congenital myopathy v0.229 TPM2 Achchuthan Shanmugasundram Tag watchlist_moi was removed from gene: TPM2.
Tag Q2_23_MOI was removed from gene: TPM2.
Tag Q2_23_NHS_review was removed from gene: TPM2.
Congenital muscular dystrophy and congenital myopathy v0.229 TNNT1 Achchuthan Shanmugasundram Tag Q2_23_MOI was removed from gene: TNNT1.
Tag Q2_23_NHS_review was removed from gene: TNNT1.
Congenital muscular dystrophy and congenital myopathy v0.229 MYH3 Achchuthan Shanmugasundram Tag Q2_23_MOI was removed from gene: MYH3.
Tag Q2_23_NHS_review was removed from gene: MYH3.
Congenital muscular dystrophy and congenital myopathy v0.229 GFER Achchuthan Shanmugasundram Tag to_be_confirmed_NHSE was removed from gene: GFER.
Congenital muscular dystrophy and congenital myopathy v0.229 CCDC78 Achchuthan Shanmugasundram Tag Q4_22_MOI was removed from gene: CCDC78.
Tag Q4_22_demote_amber was removed from gene: CCDC78.
Tag Q4_22_expert_review was removed from gene: CCDC78.
Congenital muscular dystrophy and congenital myopathy v0.229 UNC45B Achchuthan Shanmugasundram Tag Q4_22_promote_green was removed from gene: UNC45B.
Tag Q4_22_expert_review was removed from gene: UNC45B.
Tag Q4_22_NHS_review was removed from gene: UNC45B.
Congenital muscular dystrophy and congenital myopathy v0.229 POGLUT1 Achchuthan Shanmugasundram Tag Q4_22_promote_green was removed from gene: POGLUT1.
Tag Q4_22_NHS_review was removed from gene: POGLUT1.
Congenital muscular dystrophy and congenital myopathy v0.229 MYH7 Achchuthan Shanmugasundram Tag Q4_22_MOI was removed from gene: MYH7.
Tag Q2_23_NHS_review was removed from gene: MYH7.
Congenital muscular dystrophy and congenital myopathy v0.229 MLIP Achchuthan Shanmugasundram Tag Q4_22_promote_green was removed from gene: MLIP.
Congenital muscular dystrophy and congenital myopathy v0.229 GOLGA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GOLGA2.
Tag Q4_23_NHS_review was removed from gene: GOLGA2.
Congenital muscular dystrophy and congenital myopathy v0.229 COL4A1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: COL4A1.
Tag Q3_23_NHS_review was removed from gene: COL4A1.
Congenital muscular dystrophy and congenital myopathy v0.229 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_NHS_review was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Congenital muscular dystrophy and congenital myopathy v0.229 PYROXD1 Arina Puzriakova Deleted their review
Congenital muscular dystrophy and congenital myopathy v0.229 PYROXD1 Arina Puzriakova Deleted their comment
Congenital muscular dystrophy and congenital myopathy v0.229 TPM2 Arina Puzriakova changed review comment from: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Congenital muscular dystrophy and congenital myopathy v0.229 TRDN Achchuthan Shanmugasundram Tag Q2_23_promote_green was removed from gene: TRDN.
Tag Q2_23_NHS_review was removed from gene: TRDN.
Congenital muscular dystrophy and congenital myopathy v0.229 TNNT1 Arina Puzriakova changed review comment from: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Congenital muscular dystrophy and congenital myopathy v0.229 MYH7 Arina Puzriakova changed review comment from: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Congenital muscular dystrophy and congenital myopathy v0.229 MYH3 Arina Puzriakova changed review comment from: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Congenital muscular dystrophy and congenital myopathy v0.229 EMD Achchuthan Shanmugasundram Tag Q2_23_promote_green was removed from gene: EMD.
Tag Q2_23_NHS_review was removed from gene: EMD.
Tag Q2_23_expert_review was removed from gene: EMD.
Congenital muscular dystrophy and congenital myopathy v0.229 SPTBN4 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: SPTBN4.
Congenital muscular dystrophy and congenital myopathy v0.229 KY Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: KY.
Tag Q1_23_NHS_review was removed from gene: KY.
Congenital muscular dystrophy and congenital myopathy v0.229 GOSR2 Achchuthan Shanmugasundram Tag Q4_22_promote_green was removed from gene: GOSR2.
Tag Q1_23_NHS_review was removed from gene: GOSR2.
Congenital muscular dystrophy and congenital myopathy v0.229 GBE1 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: GBE1.
Tag Q1_23_NHS_review was removed from gene: GBE1.
Congenital muscular dystrophy and congenital myopathy v0.229 DTNA Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: DTNA.
Tag Q1_23_NHS_review was removed from gene: DTNA.
Congenital muscular dystrophy and congenital myopathy v0.229 DPM3 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: DPM3.
Tag Q1_23_NHS_review was removed from gene: DPM3.
Congenital muscular dystrophy and congenital myopathy v0.229 DNAJB4 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: DNAJB4.
Tag Q1_23_NHS_review was removed from gene: DNAJB4.
Congenital muscular dystrophy and congenital myopathy v0.229 COL25A1 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: COL25A1.
Tag Q1_23_NHS_review was removed from gene: COL25A1.
Congenital muscular dystrophy and congenital myopathy v0.229 COL13A1 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: COL13A1.
Tag Q1_23_NHS_review was removed from gene: COL13A1.
Congenital muscular dystrophy and congenital myopathy v0.229 BET1 Achchuthan Shanmugasundram Tag Q4_22_promote_green was removed from gene: BET1.
Tag Q1_23_NHS_review was removed from gene: BET1.
Congenital muscular dystrophy and congenital myopathy v0.229 ASCC1 Achchuthan Shanmugasundram Tag Q1_23_promote_green was removed from gene: ASCC1.
Tag Q1_23_NHS_review was removed from gene: ASCC1.
Congenital muscular dystrophy and congenital myopathy v0.229 GFER Arina Puzriakova edited their review of gene: GFER: Added comment: After further consideration by the expert group, the rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Congenital muscular dystrophy and congenital myopathy v0.229 ZC4H2 Arina Puzriakova reviewed gene: ZC4H2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Congenital muscular dystrophy and congenital myopathy v0.229 UNC45B Arina Puzriakova reviewed gene: UNC45B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 TRDN Arina Puzriakova reviewed gene: TRDN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 TPM2 Arina Puzriakova reviewed gene: TPM2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 TNNT1 Arina Puzriakova edited their review of gene: TNNT1: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 SPTBN4 Arina Puzriakova edited their review of gene: SPTBN4: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Congenital muscular dystrophy and congenital myopathy v0.229 MYH7 Arina Puzriakova edited their review of gene: MYH7: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 MYH3 Arina Puzriakova reviewed gene: MYH3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 MLIP Arina Puzriakova reviewed gene: MLIP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 LETM1 Arina Puzriakova reviewed gene: LETM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 KY Arina Puzriakova reviewed gene: KY: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 GFER Arina Puzriakova reviewed gene: GFER: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 GBE1 Arina Puzriakova reviewed gene: GBE1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 DNAJB4 Arina Puzriakova reviewed gene: DNAJB4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 COL25A1 Arina Puzriakova reviewed gene: COL25A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 COL13A1 Arina Puzriakova reviewed gene: COL13A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 CCDC78 Arina Puzriakova reviewed gene: CCDC78: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Congenital muscular dystrophy and congenital myopathy v0.229 ASCC1 Arina Puzriakova reviewed gene: ASCC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 PYROXD1 Arina Puzriakova reviewed gene: PYROXD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 POGLUT1 Arina Puzriakova reviewed gene: POGLUT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 GOSR2 Arina Puzriakova reviewed gene: GOSR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 GOLGA2 Arina Puzriakova reviewed gene: GOLGA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 EMD Arina Puzriakova reviewed gene: EMD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Congenital muscular dystrophy and congenital myopathy v0.229 DTNA Arina Puzriakova reviewed gene: DTNA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital muscular dystrophy and congenital myopathy v0.229 DPM3 Arina Puzriakova edited their review of gene: DPM3: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.229 COL4A1 Arina Puzriakova reviewed gene: COL4A1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Congenital muscular dystrophy and congenital myopathy v0.229 BET1 Arina Puzriakova reviewed gene: BET1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.227 GFER Achchuthan Shanmugasundram Source NHS GMS was added to GFER.
Source Expert Review Green was added to GFER.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 ZC4H2 Achchuthan Shanmugasundram Source Expert Review Green was added to ZC4H2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 UNC45B Achchuthan Shanmugasundram Source NHS GMS was added to UNC45B.
Source Expert Review Green was added to UNC45B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 TRDN Achchuthan Shanmugasundram Source Expert Review Green was added to TRDN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 TPM2 Achchuthan Shanmugasundram Mode of inheritance for gene TPM2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.227 TNNT1 Achchuthan Shanmugasundram Mode of inheritance for gene TNNT1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.227 SPTBN4 Achchuthan Shanmugasundram Source NHS GMS was added to SPTBN4.
Source Expert Review Green was added to SPTBN4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 MYH7 Achchuthan Shanmugasundram Mode of inheritance for gene MYH7 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.227 MYH3 Achchuthan Shanmugasundram Mode of inheritance for gene MYH3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.227 MLIP Achchuthan Shanmugasundram Source NHS GMS was added to MLIP.
Source Expert Review Green was added to MLIP.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 LETM1 Achchuthan Shanmugasundram Source NHS GMS was added to LETM1.
Source Expert Review Green was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 KY Achchuthan Shanmugasundram Source NHS GMS was added to KY.
Source Expert Review Green was added to KY.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 GBE1 Achchuthan Shanmugasundram Source NHS GMS was added to GBE1.
Source Expert Review Green was added to GBE1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 DNAJB4 Achchuthan Shanmugasundram Source NHS GMS was added to DNAJB4.
Source Expert Review Green was added to DNAJB4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 COL25A1 Achchuthan Shanmugasundram Source NHS GMS was added to COL25A1.
Source Expert Review Green was added to COL25A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 COL13A1 Achchuthan Shanmugasundram Source NHS GMS was added to COL13A1.
Source Expert Review Green was added to COL13A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 CCDC78 Achchuthan Shanmugasundram Source Expert Review Amber was added to CCDC78.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 ASCC1 Achchuthan Shanmugasundram Source NHS GMS was added to ASCC1.
Source Expert Review Green was added to ASCC1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 PYROXD1 Achchuthan Shanmugasundram Source NHS GMS was added to PYROXD1.
Congenital muscular dystrophy and congenital myopathy v0.227 POGLUT1 Achchuthan Shanmugasundram Source Expert Review Green was added to POGLUT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 GOSR2 Achchuthan Shanmugasundram Source Expert Review Green was added to GOSR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 GOLGA2 Achchuthan Shanmugasundram Source Expert Review Green was added to GOLGA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 EMD Achchuthan Shanmugasundram Source NHS GMS was added to EMD.
Source Expert Review Green was added to EMD.
Mode of inheritance for gene EMD was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 DTNA Achchuthan Shanmugasundram Source NHS GMS was added to DTNA.
Source Expert Review Green was added to DTNA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 DPM3 Achchuthan Shanmugasundram Source Expert Review Green was added to DPM3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Congenital muscular dystrophy and congenital myopathy v0.227 BET1 Achchuthan Shanmugasundram Source Expert Review Green was added to BET1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.3 SLC34A3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC34A3.
Unexplained young onset end-stage renal disease v4.3 MOCOS Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MOCOS.
Unexplained young onset end-stage renal disease v4.3 YRDC Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: YRDC.
Unexplained young onset end-stage renal disease v4.3 WNK4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: WNK4.
Unexplained young onset end-stage renal disease v4.3 WDR72 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: WDR72.
Unexplained young onset end-stage renal disease v4.3 TULP3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TULP3.
Unexplained young onset end-stage renal disease v4.3 TTR Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TTR.
Unexplained young onset end-stage renal disease v4.3 TRPM6 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TRPM6.
Unexplained young onset end-stage renal disease v4.3 TPRKB Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TPRKB.
Unexplained young onset end-stage renal disease v4.3 STRADA Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: STRADA.
Unexplained young onset end-stage renal disease v4.3 SLC5A2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC5A2.
Unexplained young onset end-stage renal disease v4.3 SLC4A4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC4A4.
Unexplained young onset end-stage renal disease v4.3 SLC4A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC4A1.
Unexplained young onset end-stage renal disease v4.3 SLC34A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC34A1.
Unexplained young onset end-stage renal disease v4.3 SLC2A2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC2A2.
Unexplained young onset end-stage renal disease v4.3 SLC12A3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC12A3.
Unexplained young onset end-stage renal disease v4.3 SLC12A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC12A1.
Unexplained young onset end-stage renal disease v4.3 SEC63 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SEC63.
Unexplained young onset end-stage renal disease v4.3 SCNN1G Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SCNN1G.
Unexplained young onset end-stage renal disease v4.3 SCNN1B Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SCNN1B.
Unexplained young onset end-stage renal disease v4.3 SCNN1A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SCNN1A.
Unexplained young onset end-stage renal disease v4.3 SARS2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SARS2.
Unexplained young onset end-stage renal disease v4.3 RRAGD Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RRAGD.
Unexplained young onset end-stage renal disease v4.3 RMND1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: RMND1.
Unexplained young onset end-stage renal disease v4.3 PRKCSH Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PRKCSH.
Unexplained young onset end-stage renal disease v4.3 PHEX Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PHEX.
Unexplained young onset end-stage renal disease v4.3 PDSS2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PDSS2.
Unexplained young onset end-stage renal disease v4.3 NR3C2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: NR3C2.
Unexplained young onset end-stage renal disease v4.3 MAGED2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MAGED2.
Unexplained young onset end-stage renal disease v4.3 LYZ Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: LYZ.
Unexplained young onset end-stage renal disease v4.3 LCAT Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: LCAT.
Unexplained young onset end-stage renal disease v4.3 KLHL3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KLHL3.
Unexplained young onset end-stage renal disease v4.3 KCNJ16 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KCNJ16.
Unexplained young onset end-stage renal disease v4.3 KCNJ10 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KCNJ10.
Unexplained young onset end-stage renal disease v4.3 KCNJ1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: KCNJ1.
Unexplained young onset end-stage renal disease v4.3 IFT27 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IFT27.
Unexplained young onset end-stage renal disease v4.3 IFT172 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IFT172.
Unexplained young onset end-stage renal disease v4.3 IFT140 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: IFT140.
Unexplained young onset end-stage renal disease v4.3 HPRT1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HPRT1.
Unexplained young onset end-stage renal disease v4.3 HNF4A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HNF4A.
Unexplained young onset end-stage renal disease v4.3 GSN Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GSN.
Unexplained young onset end-stage renal disease v4.3 GON7 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GON7.
Unexplained young onset end-stage renal disease v4.3 GNA11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: GNA11.
Unexplained young onset end-stage renal disease v4.3 FN1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FN1.
Unexplained young onset end-stage renal disease v4.3 FLCN Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FLCN.
Unexplained young onset end-stage renal disease v4.3 FGA Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FGA.
Unexplained young onset end-stage renal disease v4.3 FAM20A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FAM20A.
Unexplained young onset end-stage renal disease v4.3 FAH Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: FAH.
Unexplained young onset end-stage renal disease v4.3 DLG5 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: DLG5.
Unexplained young onset end-stage renal disease v4.3 DAAM2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: DAAM2.
Unexplained young onset end-stage renal disease v4.3 CYP24A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CYP24A1.
Unexplained young onset end-stage renal disease v4.3 CUL3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CUL3.
Unexplained young onset end-stage renal disease v4.3 CNNM2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CNNM2.
Unexplained young onset end-stage renal disease v4.3 CLDN19 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLDN19.
Unexplained young onset end-stage renal disease v4.3 CLDN16 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLDN16.
Unexplained young onset end-stage renal disease v4.3 CLDN10 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLDN10.
Unexplained young onset end-stage renal disease v4.3 CLCNKB Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CLCNKB.
Unexplained young onset end-stage renal disease v4.3 CFHR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CFHR2.
Unexplained young onset end-stage renal disease v4.3 CD151 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CD151.
Unexplained young onset end-stage renal disease v4.3 CASR Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CASR.
Unexplained young onset end-stage renal disease v4.3 CA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CA2.
Unexplained young onset end-stage renal disease v4.3 AVPR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: AVPR2.
Unexplained young onset end-stage renal disease v4.3 ATP6V1B1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATP6V1B1.
Unexplained young onset end-stage renal disease v4.3 ATP6V0A4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATP6V0A4.
Unexplained young onset end-stage renal disease v4.3 ATP1A1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATP1A1.
Unexplained young onset end-stage renal disease v4.3 APRT Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: APRT.
Unexplained young onset end-stage renal disease v4.3 APOE Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: APOE.
Unexplained young onset end-stage renal disease v4.3 APOC2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: APOC2.
Unexplained young onset end-stage renal disease v4.3 APOA2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: APOA2.
Unexplained young onset end-stage renal disease v4.3 APOA1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: APOA1.
Unexplained young onset end-stage renal disease v4.3 AP2S1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: AP2S1.
Unexplained young onset end-stage renal disease v4.3 ALG9 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ALG9.
Unexplained young onset end-stage renal disease v4.3 ALG8 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ALG8.
Unexplained young onset end-stage renal disease v4.3 ALG5 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ALG5.
Breast cancer pertinent cancer susceptibility v2.12 CDH1 Achchuthan Shanmugasundram Classified gene: CDH1 as Red List (low evidence)
Breast cancer pertinent cancer susceptibility v2.12 CDH1 Achchuthan Shanmugasundram Gene: cdh1 has been classified as Red List (Low Evidence).
Unexplained young onset end-stage renal disease v4.3 YRDC Arina Puzriakova reviewed gene: YRDC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 WNK4 Arina Puzriakova reviewed gene: WNK4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 WDR72 Arina Puzriakova reviewed gene: WDR72: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 TULP3 Arina Puzriakova reviewed gene: TULP3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 TTR Arina Puzriakova reviewed gene: TTR: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease v4.3 TRPM6 Arina Puzriakova reviewed gene: TRPM6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 TPRKB Arina Puzriakova reviewed gene: TPRKB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 STRADA Arina Puzriakova reviewed gene: STRADA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC5A2 Arina Puzriakova reviewed gene: SLC5A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC4A4 Arina Puzriakova reviewed gene: SLC4A4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC4A1 Arina Puzriakova reviewed gene: SLC4A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC34A3 Arina Puzriakova reviewed gene: SLC34A3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC34A1 Arina Puzriakova reviewed gene: SLC34A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC2A2 Arina Puzriakova reviewed gene: SLC2A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC12A3 Arina Puzriakova reviewed gene: SLC12A3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SLC12A1 Arina Puzriakova reviewed gene: SLC12A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SEC63 Arina Puzriakova reviewed gene: SEC63: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 SCNN1G Arina Puzriakova reviewed gene: SCNN1G: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SCNN1B Arina Puzriakova reviewed gene: SCNN1B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SCNN1A Arina Puzriakova reviewed gene: SCNN1A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 SARS2 Arina Puzriakova reviewed gene: SARS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 RRAGD Arina Puzriakova reviewed gene: RRAGD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 RMND1 Arina Puzriakova reviewed gene: RMND1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 PRKCSH Arina Puzriakova reviewed gene: PRKCSH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 PHEX Arina Puzriakova reviewed gene: PHEX: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Unexplained young onset end-stage renal disease v4.3 PDSS2 Arina Puzriakova reviewed gene: PDSS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 NR3C2 Arina Puzriakova reviewed gene: NR3C2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 MOCOS Arina Puzriakova reviewed gene: MOCOS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 MAGED2 Arina Puzriakova reviewed gene: MAGED2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Unexplained young onset end-stage renal disease v4.3 LYZ Arina Puzriakova reviewed gene: LYZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 LCAT Arina Puzriakova reviewed gene: LCAT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 KLHL3 Arina Puzriakova reviewed gene: KLHL3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 KCNJ16 Arina Puzriakova reviewed gene: KCNJ16: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 KCNJ10 Arina Puzriakova reviewed gene: KCNJ10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 KCNJ1 Arina Puzriakova reviewed gene: KCNJ1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 IFT27 Arina Puzriakova reviewed gene: IFT27: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 IFT172 Arina Puzriakova reviewed gene: IFT172: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 IFT140 Arina Puzriakova reviewed gene: IFT140: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 HPRT1 Arina Puzriakova reviewed gene: HPRT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Unexplained young onset end-stage renal disease v4.3 HNF4A Arina Puzriakova reviewed gene: HNF4A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease v4.3 GSN Arina Puzriakova reviewed gene: GSN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 GON7 Arina Puzriakova reviewed gene: GON7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 GNA11 Arina Puzriakova reviewed gene: GNA11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 FN1 Arina Puzriakova reviewed gene: FN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 FLCN Arina Puzriakova reviewed gene: FLCN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 FGA Arina Puzriakova reviewed gene: FGA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 FAM20A Arina Puzriakova reviewed gene: FAM20A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 FAH Arina Puzriakova reviewed gene: FAH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 DLG5 Arina Puzriakova reviewed gene: DLG5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 DAAM2 Arina Puzriakova reviewed gene: DAAM2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CYP24A1 Arina Puzriakova reviewed gene: CYP24A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CUL3 Arina Puzriakova reviewed gene: CUL3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 CNNM2 Arina Puzriakova reviewed gene: CNNM2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CLDN19 Arina Puzriakova reviewed gene: CLDN19: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CLDN16 Arina Puzriakova reviewed gene: CLDN16: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CLDN10 Arina Puzriakova reviewed gene: CLDN10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CLCNKB Arina Puzriakova reviewed gene: CLCNKB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CFHR2 Arina Puzriakova reviewed gene: CFHR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CD151 Arina Puzriakova reviewed gene: CD151: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CASR Arina Puzriakova reviewed gene: CASR: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 CA2 Arina Puzriakova reviewed gene: CA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 AVPR2 Arina Puzriakova reviewed gene: AVPR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Unexplained young onset end-stage renal disease v4.3 ATP6V1B1 Arina Puzriakova reviewed gene: ATP6V1B1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 ATP6V0A4 Arina Puzriakova reviewed gene: ATP6V0A4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 ATP1A1 Arina Puzriakova reviewed gene: ATP1A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 APRT Arina Puzriakova reviewed gene: APRT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 APOE Arina Puzriakova reviewed gene: APOE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 APOC2 Arina Puzriakova reviewed gene: APOC2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 APOA2 Arina Puzriakova reviewed gene: APOA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 APOA1 Arina Puzriakova reviewed gene: APOA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 AP2S1 Arina Puzriakova reviewed gene: AP2S1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Unexplained young onset end-stage renal disease v4.3 ALG9 Arina Puzriakova reviewed gene: ALG9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease v4.3 ALG8 Arina Puzriakova reviewed gene: ALG8: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease v4.3 ALG5 Arina Puzriakova reviewed gene: ALG5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Unexplained young onset end-stage renal disease v4.2 YRDC Achchuthan Shanmugasundram Source Expert Review Green was added to YRDC.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 WNK4 Achchuthan Shanmugasundram Source Expert Review Green was added to WNK4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 WDR72 Achchuthan Shanmugasundram Source Expert Review Green was added to WDR72.
Source NHS GMS was added to WDR72.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 TULP3 Achchuthan Shanmugasundram Source Expert Review Green was added to TULP3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 TTR Achchuthan Shanmugasundram Source Expert Review Green was added to TTR.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 TRPM6 Achchuthan Shanmugasundram Source Expert Review Green was added to TRPM6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 TPRKB Achchuthan Shanmugasundram Source Expert Review Green was added to TPRKB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 STRADA Achchuthan Shanmugasundram Source Expert Review Green was added to STRADA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC5A2 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC5A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC4A4 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC4A4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC4A1 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC4A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC34A3 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC34A3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC34A1 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC34A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC2A2 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC2A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC12A3 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC12A3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SLC12A1 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC12A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SEC63 Achchuthan Shanmugasundram Source Expert Review Green was added to SEC63.
Source NHS GMS was added to SEC63.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SCNN1G Achchuthan Shanmugasundram Source Expert Review Green was added to SCNN1G.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SCNN1B Achchuthan Shanmugasundram Source Expert Review Green was added to SCNN1B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SCNN1A Achchuthan Shanmugasundram Source Expert Review Green was added to SCNN1A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 SARS2 Achchuthan Shanmugasundram Source Expert Review Green was added to SARS2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 RRAGD Achchuthan Shanmugasundram Source Expert Review Green was added to RRAGD.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 RMND1 Achchuthan Shanmugasundram Source Expert Review Green was added to RMND1.
Source NHS GMS was added to RMND1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 PRKCSH Achchuthan Shanmugasundram Source Expert Review Green was added to PRKCSH.
Source NHS GMS was added to PRKCSH.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 PHEX Achchuthan Shanmugasundram Source Expert Review Green was added to PHEX.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 PDSS2 Achchuthan Shanmugasundram Source Expert Review Green was added to PDSS2.
Source NHS GMS was added to PDSS2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 NR3C2 Achchuthan Shanmugasundram Source Expert Review Green was added to NR3C2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 MOCOS Achchuthan Shanmugasundram Source Expert Review Green was added to MOCOS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 MAGED2 Achchuthan Shanmugasundram Source Expert Review Green was added to MAGED2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 LYZ Achchuthan Shanmugasundram Source Expert Review Green was added to LYZ.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 LCAT Achchuthan Shanmugasundram Source Expert Review Green was added to LCAT.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 KLHL3 Achchuthan Shanmugasundram Source Expert Review Green was added to KLHL3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 KCNJ16 Achchuthan Shanmugasundram Source Expert Review Green was added to KCNJ16.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 KCNJ10 Achchuthan Shanmugasundram Source Expert Review Green was added to KCNJ10.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 KCNJ1 Achchuthan Shanmugasundram Source Expert Review Green was added to KCNJ1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 IFT27 Achchuthan Shanmugasundram Source Expert Review Green was added to IFT27.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 IFT172 Achchuthan Shanmugasundram Source Expert Review Green was added to IFT172.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 IFT140 Achchuthan Shanmugasundram Source Expert Review Green was added to IFT140.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 HPRT1 Achchuthan Shanmugasundram Source Expert Review Green was added to HPRT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 HNF4A Achchuthan Shanmugasundram Source Expert Review Green was added to HNF4A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 GSN Achchuthan Shanmugasundram Source Expert Review Green was added to GSN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 GON7 Achchuthan Shanmugasundram Source Expert Review Green was added to GON7.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 GNA11 Achchuthan Shanmugasundram Source Expert Review Green was added to GNA11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 FN1 Achchuthan Shanmugasundram Source Expert Review Green was added to FN1.
Source NHS GMS was added to FN1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 FLCN Achchuthan Shanmugasundram Source Expert Review Green was added to FLCN.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 FGA Achchuthan Shanmugasundram Source Expert Review Green was added to FGA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 FAM20A Achchuthan Shanmugasundram Source Expert Review Green was added to FAM20A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 FAH Achchuthan Shanmugasundram Source Expert Review Green was added to FAH.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 DLG5 Achchuthan Shanmugasundram Source Expert Review Green was added to DLG5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 DAAM2 Achchuthan Shanmugasundram Source Expert Review Green was added to DAAM2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CYP24A1 Achchuthan Shanmugasundram Source Expert Review Green was added to CYP24A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CUL3 Achchuthan Shanmugasundram Source Expert Review Green was added to CUL3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CNNM2 Achchuthan Shanmugasundram Source Expert Review Green was added to CNNM2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CLDN19 Achchuthan Shanmugasundram Source Expert Review Green was added to CLDN19.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CLDN16 Achchuthan Shanmugasundram Source Expert Review Green was added to CLDN16.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CLDN10 Achchuthan Shanmugasundram Source Expert Review Green was added to CLDN10.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CLCNKB Achchuthan Shanmugasundram Source Expert Review Green was added to CLCNKB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CFHR2 Achchuthan Shanmugasundram Source Expert Review Green was added to CFHR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CD151 Achchuthan Shanmugasundram Source Expert Review Green was added to CD151.
Source NHS GMS was added to CD151.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CASR Achchuthan Shanmugasundram Source Expert Review Green was added to CASR.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 CA2 Achchuthan Shanmugasundram Source Expert Review Green was added to CA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 AVPR2 Achchuthan Shanmugasundram Source Expert Review Green was added to AVPR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ATP6V1B1 Achchuthan Shanmugasundram Source Expert Review Green was added to ATP6V1B1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ATP6V0A4 Achchuthan Shanmugasundram Source Expert Review Green was added to ATP6V0A4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ATP1A1 Achchuthan Shanmugasundram Source Expert Review Green was added to ATP1A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 APRT Achchuthan Shanmugasundram Source Expert Review Green was added to APRT.
Source NHS GMS was added to APRT.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 APOE Achchuthan Shanmugasundram Source Expert Review Green was added to APOE.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 APOC2 Achchuthan Shanmugasundram Source Expert Review Green was added to APOC2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 APOA2 Achchuthan Shanmugasundram Source Expert Review Green was added to APOA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 APOA1 Achchuthan Shanmugasundram Source Expert Review Green was added to APOA1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 AP2S1 Achchuthan Shanmugasundram Source Expert Review Green was added to AP2S1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ALG9 Achchuthan Shanmugasundram Source Expert Review Green was added to ALG9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ALG8 Achchuthan Shanmugasundram Source Expert Review Green was added to ALG8.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Unexplained young onset end-stage renal disease v4.2 ALG5 Achchuthan Shanmugasundram Source Expert Review Green was added to ALG5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Amelogenesis imperfecta v3.3 AMBN Claire Smith edited their review of gene: AMBN: Added comment: PMID: 38058155 identifies AMBN variants that appear to cause disease in an autosomal dominant fashion.
One family has a dominant family history spanning 4 generations, and the likely causative variant in this family was also identified as monoallelic/heterozygous in 2 other apparently unrelated individuals with isolated AI.; Changed publications to: PMID: 24858907, 26502894, 38058155; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Structural eye disease v3.79 SMG8 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: SMG8.
Tag Q4_23_NHS_review was removed from gene: SMG8.
Structural eye disease v3.79 SLC25A24 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: SLC25A24.
Tag Q4_23_NHS_review was removed from gene: SLC25A24.
Structural eye disease v3.79 RHOA Arina Puzriakova Tag Q4_23_promote_green was removed from gene: RHOA.
Tag Q4_23_NHS_review was removed from gene: RHOA.
Structural eye disease v3.79 OFD1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: OFD1.
Tag Q3_23_NHS_review was removed from gene: OFD1.
Breast cancer pertinent cancer susceptibility v2.11 CDH1 Achchuthan Shanmugasundram Classified gene: CDH1 as Amber List (moderate evidence)
Breast cancer pertinent cancer susceptibility v2.11 CDH1 Achchuthan Shanmugasundram Gene: cdh1 has been classified as Amber List (Moderate Evidence).
Structural eye disease v3.79 NUP188 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: NUP188.
Tag Q4_23_NHS_review was removed from gene: NUP188.
Structural eye disease v3.79 MIR204 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: MIR204.
Tag Q3_23_NHS_review was removed from gene: MIR204.
Breast cancer pertinent cancer susceptibility v2.10 CDH1 Achchuthan Shanmugasundram Classified gene: CDH1 as Red List (low evidence)
Breast cancer pertinent cancer susceptibility v2.10 CDH1 Achchuthan Shanmugasundram Gene: cdh1 has been classified as Red List (Low Evidence).
Breast cancer pertinent cancer susceptibility v2.9 CDH1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CDH1.
Tag Q3_23_expert_review was removed from gene: CDH1.
Structural eye disease v3.79 KIF11 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: KIF11.
Tag Q4_23_NHS_review was removed from gene: KIF11.
Structural eye disease v3.79 KIAA0586 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: KIAA0586.
Tag Q4_23_NHS_review was removed from gene: KIAA0586.
Structural eye disease v3.79 KDM6A Arina Puzriakova Tag Q4_23_promote_green was removed from gene: KDM6A.
Tag Q4_23_NHS_review was removed from gene: KDM6A.
Structural eye disease v3.79 EPHA2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: EPHA2.
Tag Q4_23_MOI was removed from gene: EPHA2.
Tag Q4_23_NHS_review was removed from gene: EPHA2.
Amelogenesis imperfecta v3.3 PLXNB2 Claire Smith changed review comment from: PMID: 38458752 Smith et al. (in press) report 8 patients in 6 families with rare biallelic pathogenic variants in PLXNB2 as a cause of a new autosomal recessive, phenotypically diverse syndrome with AI and sensorineural hearing loss as core features. Intellectual disability, ocular disease, ear developmental abnormalities and lymphoedema were also present in multiple cases.
Sources: Literature, Expert Review; to: PMID: 38458752 Smith et al. (in press) report 8 patients in 6 families with rare biallelic pathogenic variants in PLXNB2 as a cause of a new autosomal recessive, phenotypically diverse syndrome with AI and sensorineural hearing loss as core features. Intellectual disability, ocular disease, ear developmental abnormalities and lymphoedema were also present in multiple cases.
Sources: Literature, Expert Review

Personal communication with Roland Friedel and Christian Junquiera-Alves regarding their findings in their Plxnb2-/- mouse model after publication of human patients with PLXNB2 variants: "We had made also initial observations in the PB2 KO mouse on cochlear defects and tooth malformations that looked interesting, but we did not follow up as I focused on cerebellar development. Now these findings look in retrospect much more exciting considering your data."
Structural eye disease v3.79 CRYBB2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: CRYBB2.
Tag Q4_23_NHS_review was removed from gene: CRYBB2.
Structural eye disease v3.79 BMPR1B Arina Puzriakova Tag Q4_23_promote_green was removed from gene: BMPR1B.
Tag Q4_23_NHS_review was removed from gene: BMPR1B.
Structural eye disease v3.79 ARHGAP35 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: ARHGAP35.
Tag Q4_23_NHS_review was removed from gene: ARHGAP35.
Structural eye disease v3.79 ANK3 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: ANK3.
Tag Q4_23_NHS_review was removed from gene: ANK3.
Structural eye disease v3.79 ALX1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: ALX1.
Tag Q3_23_NHS_review was removed from gene: ALX1.
Structural eye disease v3.79 SMG8 Arina Puzriakova reviewed gene: SMG8: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v3.79 SLC25A24 Arina Puzriakova reviewed gene: SLC25A24: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 RHOA Arina Puzriakova reviewed gene: RHOA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Structural eye disease v3.79 OFD1 Arina Puzriakova reviewed gene: OFD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Structural eye disease v3.79 NUP188 Arina Puzriakova reviewed gene: NUP188: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v3.79 MIR204 Arina Puzriakova reviewed gene: MIR204: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 KIF11 Arina Puzriakova reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 KIAA0586 Arina Puzriakova reviewed gene: KIAA0586: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v3.79 KDM6A Arina Puzriakova reviewed gene: KDM6A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Structural eye disease v3.79 EPHA2 Arina Puzriakova reviewed gene: EPHA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Structural eye disease v3.79 CRYBB2 Arina Puzriakova reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 BMPR1B Arina Puzriakova reviewed gene: BMPR1B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 ARHGAP35 Arina Puzriakova reviewed gene: ARHGAP35: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 ANK3 Arina Puzriakova reviewed gene: ANK3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v3.79 ALX1 Arina Puzriakova reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v3.78 SMG8 Arina Puzriakova Source NHS GMS was added to SMG8.
Source Expert Review Green was added to SMG8.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 SLC25A24 Arina Puzriakova Source Expert Review Green was added to SLC25A24.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 RHOA Arina Puzriakova Source NHS GMS was added to RHOA.
Source Expert Review Green was added to RHOA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 OFD1 Arina Puzriakova Source Expert Review Green was added to OFD1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 NUP188 Arina Puzriakova Source NHS GMS was added to NUP188.
Source Expert Review Green was added to NUP188.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 MIR204 Arina Puzriakova Source Expert Review Green was added to MIR204.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 KIF11 Arina Puzriakova Source Expert Review Green was added to KIF11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 KIAA0586 Arina Puzriakova Source NHS GMS was added to KIAA0586.
Source Expert Review Green was added to KIAA0586.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 KDM6A Arina Puzriakova Source Expert Review Green was added to KDM6A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 EPHA2 Arina Puzriakova Source Expert Review Green was added to EPHA2.
Mode of inheritance for gene EPHA2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 CRYBB2 Arina Puzriakova Source Expert Review Green was added to CRYBB2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 BMPR1B Arina Puzriakova Source NHS GMS was added to BMPR1B.
Source Expert Review Green was added to BMPR1B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 ARHGAP35 Arina Puzriakova Source NHS GMS was added to ARHGAP35.
Source Expert Review Green was added to ARHGAP35.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 ANK3 Arina Puzriakova Source NHS GMS was added to ANK3.
Source Expert Review Green was added to ANK3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.78 ALX1 Arina Puzriakova Source Expert Review Green was added to ALX1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Breast cancer pertinent cancer susceptibility v2.9 ATRIP Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATRIP.
Tag Q4_23_expert_review was removed from gene: ATRIP.
Amelogenesis imperfecta v3.3 PLXNB2 Claire Smith gene: PLXNB2 was added
gene: PLXNB2 was added to Amelogenesis imperfecta. Sources: Literature,Expert Review
Mode of inheritance for gene: PLXNB2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLXNB2 were set to PMID: 38458752
Phenotypes for gene: PLXNB2 were set to Amelogenesis imperfecta; sensorineural hearing loss
Penetrance for gene: PLXNB2 were set to unknown
Review for gene: PLXNB2 was set to GREEN
Added comment: PMID: 38458752 Smith et al. (in press) report 8 patients in 6 families with rare biallelic pathogenic variants in PLXNB2 as a cause of a new autosomal recessive, phenotypically diverse syndrome with AI and sensorineural hearing loss as core features. Intellectual disability, ocular disease, ear developmental abnormalities and lymphoedema were also present in multiple cases.
Sources: Literature, Expert Review
Breast cancer pertinent cancer susceptibility v2.9 CDH1 Arina Puzriakova edited their review of gene: CDH1: Added comment: After NHS Genomic Medicine Service consideration, this gene has not been made Green and has been rated as Red. Additional comments from reviewing GLHs: 'There is a well established association of this gene withpredisposition to lobular breast cancer, but it presents huge problems when it is identified outside the context of a relevant family history. The UK Cancer genetics community do not want to add this gene to any general breast cancer susceptibility panels hence are extremely reluctant to test this gene outside of the already existing R215 criteria'; Changed rating: RED; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Breast cancer pertinent cancer susceptibility v2.9 ATRIP Arina Puzriakova edited their review of gene: ATRIP: Added comment: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remains Amber. Additional comments from reviewing GLHs: 'Whilst the referenced paper does support an association with breast cancer, more studies are needed before we can consider adding this gene to any panel. The referenced paper itself comments that further replication in larger datasets is necessary to provide figures on lifetime risk, to better define the association with breast cancer and the clinic-pathological characteristics of tumors in variant carriers . Without this important information, it is too early to add the gene to a breast cancer susceptibility panel'; Changed rating: AMBER; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v5.4 RPE65 Arina Puzriakova Tag Q4_23_MOI was removed from gene: RPE65.
Retinal disorders v5.4 PYGM Arina Puzriakova Tag Q3_23_promote_green was removed from gene: PYGM.
Tag Q3_23_NHS_review was removed from gene: PYGM.
Retinal disorders v5.4 NBAS Arina Puzriakova Tag Q3_23_promote_green was removed from gene: NBAS.
Tag Q3_23_NHS_review was removed from gene: NBAS.
Retinal disorders v5.4 MVK Arina Puzriakova Tag Q4_23_promote_green was removed from gene: MVK.
Tag Q4_23_NHS_review was removed from gene: MVK.
Retinal disorders v5.4 MPDZ Arina Puzriakova Tag Q3_23_promote_green was removed from gene: MPDZ.
Tag Q3_23_NHS_review was removed from gene: MPDZ.
Retinal disorders v5.4 MIR204 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: MIR204.
Tag Q3_23_NHS_review was removed from gene: MIR204.
Retinal disorders v5.4 MCOLN1 Arina Puzriakova Phenotypes for gene: MCOLN1 were changed from to Mucolipidosis IV, OMIM:252650
Retinal disorders v5.3 MCOLN1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: MCOLN1.
Retinal disorders v5.3 DYNC2H1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: DYNC2H1.
Retinal disorders v5.3 CTNND1 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: CTNND1.
Retinal disorders v5.3 CFAP20 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: CFAP20.
Retinal disorders v5.3 RPE65 Arina Puzriakova Mode of inheritance for gene RPE65 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Retinal disorders v5.3 PYGM Arina Puzriakova Source NHS GMS was added to PYGM.
Source Expert Review Green was added to PYGM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 NBAS Arina Puzriakova Source Expert Review Green was added to NBAS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 MVK Arina Puzriakova Source Expert Review Green was added to MVK.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 MPDZ Arina Puzriakova Source NHS GMS was added to MPDZ.
Source Expert Review Green was added to MPDZ.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 MIR204 Arina Puzriakova Source Expert Review Green was added to MIR204.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 MCOLN1 Arina Puzriakova Source NHS GMS was added to MCOLN1.
Source Expert Review Green was added to MCOLN1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 DYNC2H1 Arina Puzriakova Source NHS GMS was added to DYNC2H1.
Source Expert Review Green was added to DYNC2H1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 CTNND1 Arina Puzriakova Source NHS GMS was added to CTNND1.
Source Expert Review Green was added to CTNND1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.3 CFAP20 Arina Puzriakova Source NHS GMS was added to CFAP20.
Source Expert Review Green was added to CFAP20.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v5.2 RPE65 Arina Puzriakova edited their review of gene: RPE65: Added comment: The mode of inheritance of this gene has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Retinal disorders v5.2 PYGM Arina Puzriakova reviewed gene: PYGM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 NBAS Arina Puzriakova reviewed gene: NBAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 MVK Arina Puzriakova reviewed gene: MVK: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 MPDZ Arina Puzriakova reviewed gene: MPDZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 MIR204 Arina Puzriakova reviewed gene: MIR204: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v5.2 MCOLN1 Arina Puzriakova reviewed gene: MCOLN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 DYNC2H1 Arina Puzriakova reviewed gene: DYNC2H1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v5.2 CTNND1 Arina Puzriakova reviewed gene: CTNND1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v5.2 CFAP20 Arina Puzriakova reviewed gene: CFAP20: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 SCN8A Achchuthan Shanmugasundram Tag for-review was removed from gene: SCN8A.
Tag to_be_confirmed_NHSE was removed from gene: SCN8A.
Early onset or syndromic epilepsy v5.6 CACNB4 Achchuthan Shanmugasundram Tag Q4_23_demote_red was removed from gene: CACNB4.
Tag Q4_23_expert_review was removed from gene: CACNB4.
Early onset or syndromic epilepsy v5.6 ZBTB47 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ZBTB47.
Early onset or syndromic epilepsy v5.6 TRIT1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TRIT1.
Early onset or syndromic epilepsy v5.6 SHQ1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SHQ1.
Early onset or syndromic epilepsy v5.6 PTCD3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PTCD3.
Early onset or syndromic epilepsy v5.6 PLA2G6 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PLA2G6.
Early onset or syndromic epilepsy v5.6 PIGM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PIGM.
Early onset or syndromic epilepsy v5.6 MAST4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MAST4.
Early onset or syndromic epilepsy v5.6 HECTD4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HECTD4.
Early onset or syndromic epilepsy v5.6 ASL Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ASL.
Tag Q4_23_NHS_review was removed from gene: ASL.
Early onset or syndromic epilepsy v5.6 ARF3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ARF3.
Bilateral congenital or childhood onset cataracts v4.14 LETM1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Bilateral congenital or childhood onset cataracts v4.14 EPHA2 Arina Puzriakova Tag Q4_23_MOI was removed from gene: EPHA2.
Early onset or syndromic epilepsy v5.6 AGO1 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: AGO1.
Bilateral congenital or childhood onset cataracts v4.14 LETM1 Arina Puzriakova reviewed gene: LETM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Bilateral congenital or childhood onset cataracts v4.14 EPHA2 Arina Puzriakova reviewed gene: EPHA2: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Bilateral congenital or childhood onset cataracts v4.13 LETM1 Arina Puzriakova Source NHS GMS was added to LETM1.
Source Expert Review Green was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Bilateral congenital or childhood onset cataracts v4.13 EPHA2 Arina Puzriakova Source NHS GMS was added to EPHA2.
Mode of inheritance for gene EPHA2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 U2AF2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: U2AF2.
Early onset or syndromic epilepsy v5.6 TMEM63B Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TMEM63B.
White matter disorders and cerebral calcification - narrow panel v4.3 PPFIBP1 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: PPFIBP1.
White matter disorders and cerebral calcification - narrow panel v4.3 ESAM Arina Puzriakova Tag Q3_23_promote_green was removed from gene: ESAM.
Early onset or syndromic epilepsy v5.6 RAB5C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: RAB5C.
Early onset or syndromic epilepsy v5.6 PPP1R3F Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PPP1R3F.
Early onset or syndromic epilepsy v5.6 PIP5K1C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PIP5K1C.
White matter disorders and cerebral calcification - narrow panel v4.3 PPFIBP1 Arina Puzriakova reviewed gene: PPFIBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
White matter disorders and cerebral calcification - narrow panel v4.3 ESAM Arina Puzriakova reviewed gene: ESAM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 PABPC1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PABPC1.
Tag Q3_23_MOI was removed from gene: PABPC1.
White matter disorders and cerebral calcification - narrow panel v4.2 PPFIBP1 Arina Puzriakova Source Expert Review Green was added to PPFIBP1.
Source NHS GMS was added to PPFIBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
White matter disorders and cerebral calcification - narrow panel v4.2 ESAM Arina Puzriakova Source Expert Review Green was added to ESAM.
Source NHS GMS was added to ESAM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.6 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Early onset or syndromic epilepsy v5.6 KDM6B Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: KDM6B.
Early onset or syndromic epilepsy v5.6 KCNH5 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: KCNH5.
Intellectual disability v6.9 DPP6 Arina Puzriakova Phenotypes for gene: DPP6 were changed from autosomal dominant microcephaly and mental retardation; Mental retardation, autosomal dominant 33, 616311 to Intellectual developmental disorder, autosomal dominant 33, OMIM:616311
Early onset or syndromic epilepsy v5.6 ESAM Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ESAM.
Early onset or syndromic epilepsy v5.6 EIF4A2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: EIF4A2.
Early onset or syndromic epilepsy v5.6 DNAJC6 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DNAJC6.
Severe microcephaly v5.7 DPP6 Arina Puzriakova Phenotypes for gene: DPP6 were changed from MCPH; primary microcephaly; autosomal dominant microcephaly and mental retardation; Mental retardation, autosomal dominant 33, 616311 to Intellectual developmental disorder, autosomal dominant 33, OMIM:616311
Intellectual disability v6.8 TTI1 Arina Puzriakova Added comment: Comment on phenotypes: Relevant phenotype now listed in OMIM (Neurodevelopmental disorder with microcephaly and movement abnormalities, OMIM:620445)
Intellectual disability v6.8 TTI1 Arina Puzriakova Phenotypes for gene: TTI1 were changed from neurodevelopmental disorder with microcephaly to Neurodevelopmental disorder with microcephaly and movement abnormalities, OMIM:620445
Severe microcephaly v5.6 DPP6 Arina Puzriakova Tag to_be_confirmed_NHSE was removed from gene: DPP6.
Severe microcephaly v5.6 TTI1 Arina Puzriakova Added comment: Comment on phenotypes: Relevant phenotype now listed in OMIM (Neurodevelopmental disorder with microcephaly and movement abnormalities, OMIM:620445)
Severe microcephaly v5.6 TTI1 Arina Puzriakova Phenotypes for gene: TTI1 were changed from neurodevelopmental disorder with microcephaly to Neurodevelopmental disorder with microcephaly and movement abnormalities, OMIM:620445
Severe microcephaly v5.5 TTI1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: TTI1.
Severe microcephaly v5.5 PPFIBP1 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: PPFIBP1.
Early onset or syndromic epilepsy v5.6 CRELD1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CRELD1.
Severe microcephaly v5.5 NSD2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: NSD2.
Severe microcephaly v5.5 MECP2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: MECP2.
Severe microcephaly v5.5 KMT2B Arina Puzriakova Tag Q4_23_promote_green was removed from gene: KMT2B.
Severe microcephaly v5.5 BUB1 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: BUB1.
Severe microcephaly v5.5 ATP6V0C Arina Puzriakova Tag Q3_23_promote_green was removed from gene: ATP6V0C.
Tag Q3_23_NHS_review was removed from gene: ATP6V0C.
Severe microcephaly v5.5 ARF3 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: ARF3.
Early onset or syndromic epilepsy v5.6 CNOT9 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CNOT9.
Early onset or syndromic epilepsy v5.6 ATP6V0C Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ATP6V0C.
Tag Q3_23_NHS_review was removed from gene: ATP6V0C.
Severe microcephaly v5.5 TTI1 Arina Puzriakova Source Expert Review Green was added to TTI1.
Source NHS GMS was added to TTI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 PPFIBP1 Arina Puzriakova Source Expert Review Green was added to PPFIBP1.
Source NHS GMS was added to PPFIBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 NSD2 Arina Puzriakova Source Expert Review Green was added to NSD2.
Source NHS GMS was added to NSD2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 MECP2 Arina Puzriakova Source Expert Review Green was added to MECP2.
Source NHS GMS was added to MECP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 KMT2B Arina Puzriakova Source Expert Review Green was added to KMT2B.
Source NHS GMS was added to KMT2B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 DPP6 Arina Puzriakova Source Expert Review Amber was added to DPP6.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Severe microcephaly v5.5 BUB1 Arina Puzriakova Source Expert Review Green was added to BUB1.
Source NHS GMS was added to BUB1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 ATP6V0C Arina Puzriakova Source Expert Review Green was added to ATP6V0C.
Source NHS GMS was added to ATP6V0C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.5 ARF3 Arina Puzriakova Source Expert Review Green was added to ARF3.
Source NHS GMS was added to ARF3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Severe microcephaly v5.4 DPP6 Arina Puzriakova reviewed gene: DPP6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe microcephaly v5.4 TTI1 Arina Puzriakova reviewed gene: TTI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Severe microcephaly v5.4 PPFIBP1 Arina Puzriakova reviewed gene: PPFIBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Severe microcephaly v5.4 NSD2 Arina Puzriakova reviewed gene: NSD2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Severe microcephaly v5.4 MECP2 Arina Puzriakova reviewed gene: MECP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Severe microcephaly v5.4 KMT2B Arina Puzriakova commented on gene: KMT2B: The rating of this gene has been updated to Green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.
Severe microcephaly v5.4 BUB1 Arina Puzriakova edited their review of gene: BUB1: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Severe microcephaly v5.4 ATP6V0C Arina Puzriakova reviewed gene: ATP6V0C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Severe microcephaly v5.4 ARF3 Arina Puzriakova reviewed gene: ARF3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Early onset or syndromic epilepsy v5.6 SLC5A6 Eleanor Williams reviewed gene: SLC5A6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Early onset or syndromic epilepsy v5.6 ZBTB47 Eleanor Williams reviewed gene: ZBTB47: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 U2AF2 Eleanor Williams reviewed gene: U2AF2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 TRIT1 Eleanor Williams edited their review of gene: TRIT1: Added comment: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Early onset or syndromic epilepsy v5.6 TMEM63B Eleanor Williams reviewed gene: TMEM63B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 SHQ1 Eleanor Williams reviewed gene: SHQ1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 SCN8A Eleanor Williams reviewed gene: SCN8A: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 RAB5C Eleanor Williams reviewed gene: RAB5C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 PTCD3 Eleanor Williams reviewed gene: PTCD3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 PPP1R3F Eleanor Williams reviewed gene: PPP1R3F: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Early onset or syndromic epilepsy v5.6 PLA2G6 Eleanor Williams reviewed gene: PLA2G6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 PIP5K1C Eleanor Williams reviewed gene: PIP5K1C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 PIGM Eleanor Williams reviewed gene: PIGM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 PABPC1 Eleanor Williams reviewed gene: PABPC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 MAST4 Eleanor Williams reviewed gene: MAST4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 LETM1 Eleanor Williams reviewed gene: LETM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 KDM6B Eleanor Williams reviewed gene: KDM6B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 KCNH5 Eleanor Williams reviewed gene: KCNH5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 HECTD4 Eleanor Williams reviewed gene: HECTD4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 ESAM Eleanor Williams reviewed gene: ESAM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 EIF4A2 Eleanor Williams reviewed gene: EIF4A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 DNAJC6 Eleanor Williams reviewed gene: DNAJC6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 CRELD1 Eleanor Williams reviewed gene: CRELD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 CNOT9 Eleanor Williams reviewed gene: CNOT9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 CACNB4 Eleanor Williams reviewed gene: CACNB4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Early onset or syndromic epilepsy v5.6 ATP6V0C Eleanor Williams reviewed gene: ATP6V0C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v5.6 ASL Eleanor Williams edited their review of gene: ASL: Added comment: The rating of this gene has been updated togreenand the mode of inheritance set to'BIALLELIC, autosomal or pseudoautosomal'following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.6 ARF3 Eleanor Williams reviewed gene: ARF3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Early onset or syndromic epilepsy v5.6 AGO1 Eleanor Williams reviewed gene: AGO1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Early onset or syndromic epilepsy v5.5 ZBTB47 Achchuthan Shanmugasundram Source NHS GMS was added to ZBTB47.
Source Expert Review Green was added to ZBTB47.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 U2AF2 Achchuthan Shanmugasundram Source NHS GMS was added to U2AF2.
Source Expert Review Green was added to U2AF2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 TRIT1 Achchuthan Shanmugasundram Source NHS GMS was added to TRIT1.
Source Expert Review Green was added to TRIT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 TMEM63B Achchuthan Shanmugasundram Source NHS GMS was added to TMEM63B.
Source Expert Review Green was added to TMEM63B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 SLC5A6 Achchuthan Shanmugasundram Source NHS GMS was added to SLC5A6.
Early onset or syndromic epilepsy v5.5 SHQ1 Achchuthan Shanmugasundram Source NHS GMS was added to SHQ1.
Source Expert Review Green was added to SHQ1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 SCN8A Achchuthan Shanmugasundram Mode of inheritance for gene SCN8A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v5.5 RAB5C Achchuthan Shanmugasundram Source NHS GMS was added to RAB5C.
Source Expert Review Green was added to RAB5C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PTCD3 Achchuthan Shanmugasundram Source NHS GMS was added to PTCD3.
Source Expert Review Green was added to PTCD3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PPP1R3F Achchuthan Shanmugasundram Source NHS GMS was added to PPP1R3F.
Source Expert Review Green was added to PPP1R3F.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PLA2G6 Achchuthan Shanmugasundram Source NHS GMS was added to PLA2G6.
Source Expert Review Green was added to PLA2G6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PIP5K1C Achchuthan Shanmugasundram Source NHS GMS was added to PIP5K1C.
Source Expert Review Green was added to PIP5K1C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PIGM Achchuthan Shanmugasundram Source Expert Review Green was added to PIGM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 PABPC1 Achchuthan Shanmugasundram Source NHS GMS was added to PABPC1.
Source Expert Review Green was added to PABPC1.
Mode of inheritance for gene PABPC1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 MAST4 Achchuthan Shanmugasundram Source NHS GMS was added to MAST4.
Source Expert Review Green was added to MAST4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 LETM1 Achchuthan Shanmugasundram Source NHS GMS was added to LETM1.
Source Expert Review Green was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 KDM6B Achchuthan Shanmugasundram Source Expert Review Green was added to KDM6B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 KCNH5 Achchuthan Shanmugasundram Source Expert Review Green was added to KCNH5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 HECTD4 Achchuthan Shanmugasundram Source Expert Review Green was added to HECTD4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 ESAM Achchuthan Shanmugasundram Source NHS GMS was added to ESAM.
Source Expert Review Green was added to ESAM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 EIF4A2 Achchuthan Shanmugasundram Source NHS GMS was added to EIF4A2.
Source Expert Review Green was added to EIF4A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 DNAJC6 Achchuthan Shanmugasundram Source Expert Review Green was added to DNAJC6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 CRELD1 Achchuthan Shanmugasundram Source NHS GMS was added to CRELD1.
Source Expert Review Green was added to CRELD1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 CNOT9 Achchuthan Shanmugasundram Source NHS GMS was added to CNOT9.
Source Expert Review Green was added to CNOT9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 CACNB4 Achchuthan Shanmugasundram Source Expert Review Red was added to CACNB4.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Early onset or syndromic epilepsy v5.5 ATP6V0C Achchuthan Shanmugasundram Source NHS GMS was added to ATP6V0C.
Source Expert Review Green was added to ATP6V0C.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 ASL Achchuthan Shanmugasundram Source NHS GMS was added to ASL.
Source Expert Review Green was added to ASL.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 ARF3 Achchuthan Shanmugasundram Source NHS GMS was added to ARF3.
Source Expert Review Green was added to ARF3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v5.5 AGO1 Achchuthan Shanmugasundram Source NHS GMS was added to AGO1.
Source Expert Review Green was added to AGO1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Distal myopathies v4.3 SMPX Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SMPX.
Tag Q3_23_MOI was removed from gene: SMPX.
Distal myopathies v4.3 SMPX Eleanor Williams reviewed gene: SMPX: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Distal myopathies v4.2 SMPX Achchuthan Shanmugasundram Source Expert Review Green was added to SMPX.
Source NHS GMS was added to SMPX.
Mode of inheritance for gene SMPX was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary ataxia with onset in adulthood v5.3 UCHL1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: UCHL1.
Tag Q3_23_MOI was removed from gene: UCHL1.
Hereditary ataxia with onset in adulthood v5.3 TDP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TDP1.
Hereditary ataxia with onset in adulthood v5.3 UCHL1 Eleanor Williams reviewed gene: UCHL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary ataxia with onset in adulthood v5.3 TDP1 Eleanor Williams reviewed gene: TDP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary ataxia with onset in adulthood v5.2 UCHL1 Achchuthan Shanmugasundram Source Expert Review Green was added to UCHL1.
Mode of inheritance for gene UCHL1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary ataxia with onset in adulthood v5.2 TDP1 Achchuthan Shanmugasundram Source Expert Review Green was added to TDP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.3 ZC4H2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ZC4H2.
Clefting v5.3 TRRAP Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: TRRAP.
Clefting v5.3 STAG2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: STAG2.
Clefting v5.3 SMARCA4 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SMARCA4.
Clefting v5.3 PGM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PGM1.
Clefting v5.3 PGAP3 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PGAP3.
Clefting v5.3 KAT6B Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: KAT6B.
Clefting v5.3 HNRNPK Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: HNRNPK.
Clefting v5.3 GLI2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: GLI2.
Clefting v5.3 CNTNAP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: CNTNAP1.
Clefting v5.3 AMOTL1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: AMOTL1.
Clefting v5.3 ALX1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: ALX1.
Clefting v5.3 ZC4H2 Sarah Leigh reviewed gene: ZC4H2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Clefting v5.3 TRRAP Sarah Leigh reviewed gene: TRRAP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Clefting v5.3 STAG2 Sarah Leigh reviewed gene: STAG2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Clefting v5.3 SMARCA4 Sarah Leigh reviewed gene: SMARCA4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Clefting v5.3 PGM1 Sarah Leigh reviewed gene: PGM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting v5.3 PGAP3 Sarah Leigh reviewed gene: PGAP3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting v5.3 KAT6B Sarah Leigh reviewed gene: KAT6B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Clefting v5.3 HNRNPK Sarah Leigh reviewed gene: HNRNPK: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Clefting v5.3 GLI2 Sarah Leigh reviewed gene: GLI2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Clefting v5.3 CNTNAP1 Sarah Leigh reviewed gene: CNTNAP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting v5.3 AMOTL1 Sarah Leigh reviewed gene: AMOTL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Clefting v5.3 ALX1 Sarah Leigh edited their review of gene: ALX1: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Clefting v5.2 ZC4H2 Achchuthan Shanmugasundram Source Expert Review Green was added to ZC4H2.
Source NHS GMS was added to ZC4H2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 TRRAP Achchuthan Shanmugasundram Source Expert Review Green was added to TRRAP.
Source NHS GMS was added to TRRAP.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 STAG2 Achchuthan Shanmugasundram Source Expert Review Green was added to STAG2.
Source NHS GMS was added to STAG2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 SMARCA4 Achchuthan Shanmugasundram Source Expert Review Green was added to SMARCA4.
Source NHS GMS was added to SMARCA4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 PGM1 Achchuthan Shanmugasundram Source Expert Review Green was added to PGM1.
Source NHS GMS was added to PGM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 PGAP3 Achchuthan Shanmugasundram Source Expert Review Green was added to PGAP3.
Source NHS GMS was added to PGAP3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 KAT6B Achchuthan Shanmugasundram Source Expert Review Green was added to KAT6B.
Source NHS GMS was added to KAT6B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 HNRNPK Achchuthan Shanmugasundram Source Expert Review Green was added to HNRNPK.
Source NHS GMS was added to HNRNPK.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 GLI2 Achchuthan Shanmugasundram Source Expert Review Green was added to GLI2.
Source NHS GMS was added to GLI2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 CNTNAP1 Achchuthan Shanmugasundram Source Expert Review Green was added to CNTNAP1.
Source NHS GMS was added to CNTNAP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 AMOTL1 Achchuthan Shanmugasundram Source Expert Review Green was added to AMOTL1.
Source NHS GMS was added to AMOTL1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Clefting v5.2 ALX1 Achchuthan Shanmugasundram Source Expert Review Green was added to ALX1.
Source NHS GMS was added to ALX1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.3 THG1L Achchuthan Shanmugasundram Tag watchlist was removed from gene: THG1L.
Tag Q4_23_promote_green was removed from gene: THG1L.
Tag Q4_23_NHS_review was removed from gene: THG1L.
Ataxia and cerebellar anomalies - narrow panel v5.3 DLG4 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: DLG4.
Ataxia and cerebellar anomalies - narrow panel v5.3 ASL Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ASL.
Tag Q4_23_NHS_review was removed from gene: ASL.
Ataxia and cerebellar anomalies - narrow panel v5.3 UCHL1 Achchuthan Shanmugasundram Tag Q3_23_MOI was removed from gene: UCHL1.
Ataxia and cerebellar anomalies - narrow panel v5.3 LETM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: LETM1.
Tag Q3_23_MOI was removed from gene: LETM1.
Ataxia and cerebellar anomalies - narrow panel v5.3 DNAJC3 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DNAJC3.
Ataxia and cerebellar anomalies - narrow panel v5.3 DAGLA Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: DAGLA.
Ataxia and cerebellar anomalies - narrow panel v5.3 AGTPBP1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: AGTPBP1.
Ataxia and cerebellar anomalies - narrow panel v5.3 UCHL1 Sarah Leigh commented on gene: UCHL1: The mode of inheritance of this gene has been updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Ataxia and cerebellar anomalies - narrow panel v5.3 THG1L Sarah Leigh reviewed gene: THG1L: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v5.3 LETM1 Sarah Leigh commented on gene: LETM1: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Ataxia and cerebellar anomalies - narrow panel v5.3 DNAJC3 Sarah Leigh reviewed gene: DNAJC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v5.3 DLG4 Sarah Leigh reviewed gene: DLG4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Ataxia and cerebellar anomalies - narrow panel v5.3 DAGLA Sarah Leigh reviewed gene: DAGLA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Ataxia and cerebellar anomalies - narrow panel v5.3 ASL Sarah Leigh reviewed gene: ASL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v5.3 AGTPBP1 Sarah Leigh reviewed gene: AGTPBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v5.2 UCHL1 Achchuthan Shanmugasundram Mode of inheritance for gene UCHL1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v5.2 THG1L Achchuthan Shanmugasundram Source Expert Review Green was added to THG1L.
Source NHS GMS was added to THG1L.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 LETM1 Achchuthan Shanmugasundram Source Expert Review Green was added to LETM1.
Source NHS GMS was added to LETM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 DNAJC3 Achchuthan Shanmugasundram Source Expert Review Green was added to DNAJC3.
Source NHS GMS was added to DNAJC3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 DLG4 Achchuthan Shanmugasundram Source Expert Review Green was added to DLG4.
Source NHS GMS was added to DLG4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 DAGLA Achchuthan Shanmugasundram Source Expert Review Green was added to DAGLA.
Source NHS GMS was added to DAGLA.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 ASL Achchuthan Shanmugasundram Source Expert Review Green was added to ASL.
Source NHS GMS was added to ASL.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v5.2 AGTPBP1 Achchuthan Shanmugasundram Source Expert Review Green was added to AGTPBP1.
Source NHS GMS was added to AGTPBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Rhabdomyolysis and metabolic muscle disorders v4.4 TAMM41 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: TAMM41.
Rhabdomyolysis and metabolic muscle disorders v4.4 PNPLA2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: PNPLA2.
Rhabdomyolysis and metabolic muscle disorders v4.4 ISCU Arina Puzriakova Phenotypes for gene: ISCU were changed from Myopathy with lactic acidosis, hereditary 255125 to Myopathy with lactic acidosis, hereditary, OMIM:255125
Rhabdomyolysis and metabolic muscle disorders v4.3 ISCU Arina Puzriakova Tag for-review was removed from gene: ISCU.
Tag to_be_confirmed_NHSE was removed from gene: ISCU.
Rhabdomyolysis and metabolic muscle disorders v4.3 ABHD5 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: ABHD5.
Rhabdomyolysis and metabolic muscle disorders v4.3 ABHD5 Arina Puzriakova edited their review of gene: ABHD5: Changed rating: GREEN
Rhabdomyolysis and metabolic muscle disorders v4.3 ABHD5 Arina Puzriakova changed review comment from: The mode of inheritance of this gene has been updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Mitochondrial disorders v6.4 ANO10 Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: ANO10.
Tag Q2_24_demote_amber tag was added to gene: ANO10.
Tag Q2_24_expert_review tag was added to gene: ANO10.
Mitochondrial disorders v6.4 BTD Achchuthan Shanmugasundram Tag Q3_23_expert_review was removed from gene: BTD.
Tag Q2_24_demote_amber tag was added to gene: BTD.
Tag Q2_24_expert_review tag was added to gene: BTD.
Rhabdomyolysis and metabolic muscle disorders v4.3 ISCU Arina Puzriakova edited their review of gene: ISCU: Added comment: The mode of inheritance of this gene has been updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and metabolic muscle disorders v4.3 TAMM41 Arina Puzriakova reviewed gene: TAMM41: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and metabolic muscle disorders v4.3 PNPLA2 Arina Puzriakova reviewed gene: PNPLA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and metabolic muscle disorders v4.3 ABHD5 Arina Puzriakova reviewed gene: ABHD5: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and metabolic muscle disorders v4.2 TAMM41 Arina Puzriakova Source Expert Review Green was added to TAMM41.
Source NHS GMS was added to TAMM41.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Rhabdomyolysis and metabolic muscle disorders v4.2 PNPLA2 Arina Puzriakova Source Expert Review Green was added to PNPLA2.
Source NHS GMS was added to PNPLA2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Rhabdomyolysis and metabolic muscle disorders v4.2 ISCU Arina Puzriakova Source NHS GMS was added to ISCU.
Mode of inheritance for gene ISCU was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and metabolic muscle disorders v4.2 ABHD5 Arina Puzriakova Source Expert Review Green was added to ABHD5.
Source NHS GMS was added to ABHD5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v5.4 HECTD4 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: HECTD4.
Malformations of cortical development v5.4 COL4A2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: COL4A2.
Tag Q4_23_NHS_review was removed from gene: COL4A2.
Intellectual disability v6.7 CASP2 Arina Puzriakova Phenotypes for gene: CASP2 were changed from neurodevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071 to Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly, OMIM:620653
DDG2P v4.3 CASP2 Arina Puzriakova Phenotypes for gene: CASP2 were changed from AUTOSOMAL RECESSIVE MENTAL RETARDATION to Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly, OMIM:620653
Malformations of cortical development v5.4 COL4A1 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: COL4A1.
Tag Q4_23_NHS_review was removed from gene: COL4A1.
Malformations of cortical development v5.4 CASP2 Arina Puzriakova Phenotypes for gene: CASP2 were changed from neurodevelopmental disorder, MONDO:0700092; hereditary cerebral malformation, MONDO:0957008 to Intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly, OMIM:620653
Malformations of cortical development v5.3 CASP2 Arina Puzriakova Tag Q4_23_promote_green was removed from gene: CASP2.
Malformations of cortical development v5.3 HECTD4 Arina Puzriakova Source Expert Review Green was added to HECTD4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v5.3 COL4A2 Arina Puzriakova Source NHS GMS was added to COL4A2.
Source Expert Review Green was added to COL4A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v5.3 COL4A1 Arina Puzriakova Source NHS GMS was added to COL4A1.
Source Expert Review Green was added to COL4A1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v5.3 CASP2 Arina Puzriakova Source NHS GMS was added to CASP2.
Source Expert Review Green was added to CASP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v5.2 HECTD4 Arina Puzriakova commented on gene: HECTD4: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.
Malformations of cortical development v5.2 COL4A2 Arina Puzriakova reviewed gene: COL4A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Malformations of cortical development v5.2 COL4A1 Arina Puzriakova reviewed gene: COL4A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Malformations of cortical development v5.2 CASP2 Arina Puzriakova reviewed gene: CASP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.4 HPDL Achchuthan Shanmugasundram Tag for-review was removed from gene: HPDL.
Tag to_be_confirmed_NHSE was removed from gene: HPDL.
Mitochondrial disorders v6.4 PTCD3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: PTCD3.
Mitochondrial disorders v6.4 TEFM Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TEFM.
Tag Q4_23_NHS_review was removed from gene: TEFM.
Mitochondrial disorders v6.4 TAMM41 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: TAMM41.
Tag Q4_23_NHS_review was removed from gene: TAMM41.
Mitochondrial disorders v6.4 SLC52A3 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC52A3.
Tag Q4_23_MOI was removed from gene: SLC52A3.
Mitochondrial disorders v6.4 SLC52A2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC52A2.
Mitochondrial disorders v6.4 SLC25A36 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: SLC25A36.
Tag Q4_23_NHS_review was removed from gene: SLC25A36.
Mitochondrial disorders v6.4 MRM2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: MRM2.
Mitochondrial disorders v6.4 HADHB Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HADHB.
Mitochondrial disorders v6.4 COX5A Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: COX5A.
Mitochondrial disorders v6.4 COX11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: COX11.
Mitochondrial disorders v6.4 ATP5E Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATP5E.
Mitochondrial disorders v6.4 SLC25A24 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC25A24.
Mitochondrial disorders v6.4 SLC25A20 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC25A20.
Mitochondrial disorders v6.4 SLC22A5 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: SLC22A5.
Mitochondrial disorders v6.4 QARS Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: QARS.
Mitochondrial disorders v6.4 PPOX Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PPOX.
Mitochondrial disorders v6.4 PLA2G6 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PLA2G6.
Mitochondrial disorders v6.4 PITRM1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PITRM1.
Mitochondrial disorders v6.4 PANK2 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: PANK2.
Mitochondrial disorders v6.4 OXCT1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: OXCT1.
Hydrocephalus v4.6 HYLS1 Arina Puzriakova Tag to_be_confirmed_NHSE was removed from gene: HYLS1.
Hydrocephalus v4.6 MYMK Arina Puzriakova Tag to_be_confirmed_NHSE was removed from gene: MYMK.
Hydrocephalus v4.6 ERF Arina Puzriakova Tag to_be_confirmed_NHSE was removed from gene: ERF.
Hydrocephalus v4.6 MYMK Arina Puzriakova reviewed gene: MYMK: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hydrocephalus v4.6 HYLS1 Arina Puzriakova reviewed gene: HYLS1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hydrocephalus v4.6 ERF Arina Puzriakova reviewed gene: ERF: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hydrocephalus v4.5 MYMK Arina Puzriakova Source Expert Review Amber was added to MYMK.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Hydrocephalus v4.5 ERF Arina Puzriakova Source Expert Review Red was added to ERF.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Mitochondrial disorders v6.4 TEFM Sarah Leigh edited their review of gene: TEFM: Changed rating: GREEN
Mitochondrial disorders v6.4 TAMM41 Sarah Leigh edited their review of gene: TAMM41: Changed rating: GREEN
Mitochondrial disorders v6.4 SLC25A36 Sarah Leigh edited their review of gene: SLC25A36: Changed rating: GREEN
Mitochondrial disorders v6.4 QARS Sarah Leigh edited their review of gene: QARS: Changed rating: GREEN
Mitochondrial disorders v6.4 PPOX Sarah Leigh edited their review of gene: PPOX: Changed rating: GREEN
Mitochondrial disorders v6.4 PANK2 Sarah Leigh edited their review of gene: PANK2: Changed rating: GREEN
Mitochondrial disorders v6.4 OXCT1 Sarah Leigh edited their review of gene: OXCT1: Changed rating: GREEN
Mitochondrial disorders v6.4 HADHB Sarah Leigh edited their review of gene: HADHB: Changed rating: GREEN
Holoprosencephaly - NOT chromosomal v4.9 DISP1 Arina Puzriakova Tag to_be_confirmed_NHSE was removed from gene: DISP1.
Holoprosencephaly - NOT chromosomal v4.9 DISP1 Arina Puzriakova changed review comment from: The rating of this gene has been updated to Amber following NHS Genomic Medicine Service approval.; to: The rating of this gene has been demoted to Amber following NHS Genomic Medicine Service approval.
Holoprosencephaly - NOT chromosomal v4.9 DISP1 Arina Puzriakova reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Holoprosencephaly - NOT chromosomal v4.8 DISP1 Arina Puzriakova Source Expert Review Amber was added to DISP1.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Mitochondrial disorders v6.3 TEFM Sarah Leigh reviewed gene: TEFM: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 TAMM41 Sarah Leigh reviewed gene: TAMM41: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 SLC52A3 Sarah Leigh commented on gene: SLC52A3: The rating of this gene has been updated to green and the mode of inheritance updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Mitochondrial disorders v6.3 SLC52A2 Sarah Leigh edited their review of gene: SLC52A2: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 SLC25A36 Sarah Leigh reviewed gene: SLC25A36: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 SLC25A24 Sarah Leigh commented on gene: SLC25A24: The rating of this gene has been updated to green and the mode of inheritance updated to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted following NHS Genomic Medicine Service approval.
Mitochondrial disorders v6.3 SLC25A20 Sarah Leigh edited their review of gene: SLC25A20: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 SLC22A5 Sarah Leigh commented on gene: SLC22A5: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Mitochondrial disorders v6.3 QARS Sarah Leigh reviewed gene: QARS: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 PTCD3 Sarah Leigh edited their review of gene: PTCD3: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 PPOX Sarah Leigh edited their review of gene: PPOX: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 PLA2G6 Sarah Leigh commented on gene: PLA2G6: The rating of this gene has been updated to green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Mitochondrial disorders v6.3 PITRM1 Sarah Leigh edited their review of gene: PITRM1: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 PANK2 Sarah Leigh reviewed gene: PANK2: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 OXCT1 Sarah Leigh edited their review of gene: OXCT1: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 MRM2 Sarah Leigh edited their review of gene: MRM2: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 HPDL Sarah Leigh edited their review of gene: HPDL: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 HADHB Sarah Leigh edited their review of gene: HADHB: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 COX5A Sarah Leigh edited their review of gene: COX5A: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 COX11 Sarah Leigh edited their review of gene: COX11: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.3 ATP5E Sarah Leigh edited their review of gene: ATP5E: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.2 TEFM Achchuthan Shanmugasundram Source NHS GMS was added to TEFM.
Source Expert Review Green was added to TEFM.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 TAMM41 Achchuthan Shanmugasundram Source NHS GMS was added to TAMM41.
Source Expert Review Green was added to TAMM41.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC52A3 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC52A3.
Mode of inheritance for gene SLC52A3 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC52A2 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC52A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC25A36 Achchuthan Shanmugasundram Source NHS GMS was added to SLC25A36.
Source Expert Review Green was added to SLC25A36.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC25A24 Achchuthan Shanmugasundram Source NHS GMS was added to SLC25A24.
Source Expert Review Green was added to SLC25A24.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC25A20 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC25A20.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 SLC22A5 Achchuthan Shanmugasundram Source Expert Review Green was added to SLC22A5.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 QARS Achchuthan Shanmugasundram Source NHS GMS was added to QARS.
Source Expert Review Green was added to QARS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 PTCD3 Achchuthan Shanmugasundram Source Expert Review Green was added to PTCD3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 PPOX Achchuthan Shanmugasundram Source Expert Review Green was added to PPOX.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 PLA2G6 Achchuthan Shanmugasundram Source NHS GMS was added to PLA2G6.
Source Expert Review Green was added to PLA2G6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 PITRM1 Achchuthan Shanmugasundram Source NHS GMS was added to PITRM1.
Source Expert Review Green was added to PITRM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 PANK2 Achchuthan Shanmugasundram Source NHS GMS was added to PANK2.
Source Expert Review Green was added to PANK2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 OXCT1 Achchuthan Shanmugasundram Source Expert Review Green was added to OXCT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 MRM2 Achchuthan Shanmugasundram Source Expert Review Green was added to MRM2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 HPDL Achchuthan Shanmugasundram Source NHS GMS was added to HPDL.
Source Expert Review Green was added to HPDL.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 HADHB Achchuthan Shanmugasundram Source Expert Review Green was added to HADHB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 COX5A Achchuthan Shanmugasundram Source NHS GMS was added to COX5A.
Source Expert Review Green was added to COX5A.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 COX11 Achchuthan Shanmugasundram Source Expert Review Green was added to COX11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v6.2 ATP5E Achchuthan Shanmugasundram Source NHS GMS was added to ATP5E.
Source Expert Review Green was added to ATP5E.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.6 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from Neurodevelopmental disorder with hypotonia, neuropathy, and deafness MIM#617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
Early onset or syndromic epilepsy v5.4 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from Neurodevelopmental disorder with hypotonia, neuropathy, and deafness MIM#617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
Monogenic hearing loss v4.41 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, 617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
DDG2P v4.2 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS, OMIM:617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
Hereditary neuropathy v1.478 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, 617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
Hereditary neuropathy or pain disorder v4.8 SPTBN4 Arina Puzriakova Phenotypes for gene: SPTBN4 were changed from Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, 617519 to Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, OMIM:617519
Hereditary neuropathy or pain disorder v4.7 SPTBN4 Arina Puzriakova Tag for-review was removed from gene: SPTBN4.
Tag to_be_confirmed_NHSE was removed from gene: SPTBN4.
Hereditary neuropathy or pain disorder v4.7 NEMF Arina Puzriakova Phenotypes for gene: NEMF were changed from Hypotonia; Axonal neuropathy; Ataxia; Abnormal brain imaging; Global developmental delay; Intellectual disability; Kyphosis; Scoliosis; Tremor; Respiratory distress to Intellectual developmental disorder with speech delay and axonal peripheral neuropathy, OMIM:619099
Hereditary neuropathy or pain disorder v4.6 NEMF Arina Puzriakova Tag watchlist was removed from gene: NEMF.
Tag for-review was removed from gene: NEMF.
Tag to_be_confirmed_NHSE was removed from gene: NEMF.
Hereditary neuropathy or pain disorder v4.6 SYT2 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: SYT2.
Hereditary neuropathy or pain disorder v4.6 SPTAN1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: SPTAN1.
Hereditary neuropathy or pain disorder v4.6 SARS Arina Puzriakova Tag Q4_23_promote_green was removed from gene: SARS.
Tag Q4_23_NHS_review was removed from gene: SARS.
Hereditary neuropathy or pain disorder v4.6 PPOX Arina Puzriakova Phenotypes for gene: PPOX were changed from Porphyria variegata, 176200; Skin photosensitivity. Acute episodes similar to AIP to Porphyria variegata, OMIM:176200; Sensory neuropathy, HP:0000763
Hereditary neuropathy or pain disorder v4.5 PPOX Arina Puzriakova Tag Q3_23_MOI was removed from gene: PPOX.
Hereditary neuropathy or pain disorder v4.5 ITPR3 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: ITPR3.
Hereditary neuropathy or pain disorder v4.5 DNAJC3 Arina Puzriakova Phenotypes for gene: DNAJC3 were changed from Cerebellar ataxia, neuropathy with SNCV, hearing loss, diabetes mellitus; Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, 616192 to Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, OMIM:616192
Hereditary neuropathy or pain disorder v4.4 DNAJC3 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: DNAJC3.
Hereditary neuropathy or pain disorder v4.4 DHX9 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: DHX9.
Hereditary neuropathy or pain disorder v4.4 DHTKD1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: DHTKD1.
Hereditary neuropathy or pain disorder v4.4 AGTPBP1 Arina Puzriakova Phenotypes for gene: AGTPBP1 were changed from Early onset cerebellar atrophy, developmental delay, and feeding and respiratory difficulties, severe motor neuronopathy; Neurodegeneration, childhood-onset, with cerebellar atrophy, 618276 to Neurodegeneration, childhood-onset, with cerebellar atrophy, OMIM:618276
Hereditary neuropathy or pain disorder v4.3 AGTPBP1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: AGTPBP1.
Hereditary neuropathy or pain disorder v4.3 SPTBN4 Arina Puzriakova edited their review of gene: SPTBN4: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Hereditary neuropathy or pain disorder v4.3 NEMF Arina Puzriakova edited their review of gene: NEMF: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.3 SYT2 Arina Puzriakova reviewed gene: SYT2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 SPTAN1 Arina Puzriakova reviewed gene: SPTAN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 SLC12A6 Arina Puzriakova edited their review of gene: SLC12A6: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.3 SARS Arina Puzriakova reviewed gene: SARS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 PPOX Arina Puzriakova reviewed gene: PPOX: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.3 ITPR3 Arina Puzriakova reviewed gene: ITPR3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 DNAJC3 Arina Puzriakova reviewed gene: DNAJC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.3 DHX9 Arina Puzriakova edited their review of gene: DHX9: Added comment: The rating of this gene has been updated to Green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted' following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 DHTKD1 Arina Puzriakova reviewed gene: DHTKD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary neuropathy or pain disorder v4.3 AGTPBP1 Arina Puzriakova reviewed gene: AGTPBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.2 SYT2 Arina Puzriakova Source Expert Review Green was added to SYT2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 SPTBN4 Arina Puzriakova Source NHS GMS was added to SPTBN4.
Source Expert Review Green was added to SPTBN4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 SPTAN1 Arina Puzriakova Source NHS GMS was added to SPTAN1.
Source Expert Review Green was added to SPTAN1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 SLC12A6 Arina Puzriakova Source Expert Review Green was added to SLC12A6.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 SARS Arina Puzriakova Source NHS GMS was added to SARS.
Source Expert Review Green was added to SARS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 PPOX Arina Puzriakova Mode of inheritance for gene PPOX was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v4.2 NEMF Arina Puzriakova Source NHS GMS was added to NEMF.
Source Expert Review Green was added to NEMF.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 ITPR3 Arina Puzriakova Source NHS GMS was added to ITPR3.
Source Expert Review Green was added to ITPR3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 DNAJC3 Arina Puzriakova Source Expert Review Green was added to DNAJC3.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 DHX9 Arina Puzriakova Source NHS GMS was added to DHX9.
Source Expert Review Green was added to DHX9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 DHTKD1 Arina Puzriakova Source Expert Review Green was added to DHTKD1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Hereditary neuropathy or pain disorder v4.2 AGTPBP1 Arina Puzriakova Source Expert Review Green was added to AGTPBP1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Limb disorders v5.2 ISCA-37467-Gain Arina Puzriakova edited their review of Region: ISCA-37467-Gain: Added comment: The rating of this region has been updated to Green and the mode of inheritance set to 'MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown' following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Intellectual disability v6.5 ISCA-46292-Loss Arina Puzriakova reviewed Region: ISCA-46292-Loss: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Severe microcephaly v5.3 ISCA-46743-Loss Arina Puzriakova reviewed Region: ISCA-46743-Loss: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Intellectual disability v6.5 ISCA-46743-Loss Arina Puzriakova changed review comment from: The rating of this region has been updated to Green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)' following NHS Genomic Medicine Service approval. Evidence: multiple unrelated cases curated in ClinGen plus several others - sufficient evidence for this region. Phenotype: syndromic intellectual disability (congenital anomalies, behavioural problems and facial dysmorphism), seizures in about 30%. Modulated phenotype in females is reported.; to: The rating of this region has been updated to Green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)' following NHS Genomic Medicine Service approval. Evidence: two cases (PMID: 30158690; 33758131) with intragenic STAG2 deletions but listed as sufficient evidence in ClinGen. Region encompasses STAG2 and some of XIAP. Phenotype: holoprosencephaly and/or developmental delay/ID based on LOF of STAG2 gene. Affected females are reported.
Early onset or syndromic epilepsy v5.3 ISCA-46743-Gain Arina Puzriakova changed review comment from: The rating of this region has been updated to Green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)' following NHS Genomic Medicine Service approval. Evidence: multiple unrelated cases curated in ClinGen plus several others - sufficient evidence for this region. Phenotype: syndromic intellectual disability (congenital anomalies, behavioural problems and facial dysmorphism). Modulated phenotype in females is reported.; to: The rating of this region has been updated to Green and the mode of inheritance set to 'X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)' following NHS Genomic Medicine Service approval. Evidence: multiple unrelated cases curated in ClinGen plus several others - sufficient evidence for this region. Phenotype: syndromic intellectual disability (congenital anomalies, behavioural problems and facial dysmorphism), seizures in about 30%. Modulated phenotype in females is reported.
Intellectual disability v6.5 ISCA-46743-Gain Arina Puzriakova reviewed Region: ISCA-46743-Gain: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Holoprosencephaly - NOT chromosomal v4.7 ISCA-46743-Loss Arina Puzriakova reviewed Region: ISCA-46743-Loss: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Intellectual disability v6.5 ISCA-46743-Loss Arina Puzriakova reviewed Region: ISCA-46743-Loss: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Early onset or syndromic epilepsy v5.3 ISCA-46743-Gain Arina Puzriakova reviewed Region: ISCA-46743-Gain: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Intellectual disability v6.5 ISCA-46292-Loss Arina Puzriakova Publications for Region: ISCA-46292-Loss were set to
Limb disorders v5.2 ISCA-37467-Gain Arina Puzriakova Tag Q3_23_promote_green was removed from Region: ISCA-37467-Gain.
Intellectual disability v6.4 ISCA-46743-Loss Arina Puzriakova Publications for Region: ISCA-46743-Loss were set to
Severe microcephaly v5.3 ISCA-46743-Loss Arina Puzriakova Publications for Region: ISCA-46743-Loss were set to
Holoprosencephaly - NOT chromosomal v4.7 ISCA-46743-Loss Arina Puzriakova Publications for Region: ISCA-46743-Loss were set to
Early onset or syndromic epilepsy v5.3 ISCA-46743-Gain Arina Puzriakova Publications for Region: ISCA-46743-Gain were set to
Intellectual disability v6.3 ISCA-46743-Gain Arina Puzriakova Publications for Region: ISCA-46743-Gain were set to
Limb disorders v5.2 ISCA-37467-Gain Arina Puzriakova Haploinsufficiency Score for ISCA-37467-Gain was changed from None to .
Source Expert Review Green was added to Region: ISCA-37467-Gain.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Intellectual disability v6.2 ISCA-46292-Loss Arina Puzriakova Region: ISCA-46292-Loss was added
Region: ISCA-46292-Loss was added to Intellectual disability. Sources: Expert Review Green,ClinGen
Mode of inheritance for Region: ISCA-46292-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe microcephaly v5.2 ISCA-46743-Loss Arina Puzriakova Region: ISCA-46743-Loss was added
Region: ISCA-46743-Loss was added to Severe microcephaly. Sources: ClinGen,Expert Review Amber
Mode of inheritance for Region: ISCA-46743-Loss was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Holoprosencephaly - NOT chromosomal v4.6 ISCA-46743-Loss Arina Puzriakova Region: ISCA-46743-Loss was added
Region: ISCA-46743-Loss was added to Holoprosencephaly - NOT chromosomal. Sources: Expert Review Green,ClinGen
Mode of inheritance for Region: ISCA-46743-Loss was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability v6.2 ISCA-46743-Loss Arina Puzriakova Region: ISCA-46743-Loss was added
Region: ISCA-46743-Loss was added to Intellectual disability. Sources: Expert Review Green,ClinGen
Mode of inheritance for Region: ISCA-46743-Loss was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Early onset or syndromic epilepsy v5.2 ISCA-46743-Gain Arina Puzriakova Region: ISCA-46743-Gain was added
Region: ISCA-46743-Gain was added to Early onset or syndromic epilepsy. Sources: Expert Review Green,ClinGen
Mode of inheritance for Region: ISCA-46743-Gain was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability v6.2 ISCA-46743-Gain Arina Puzriakova Region: ISCA-46743-Gain was added
Region: ISCA-46743-Gain was added to Intellectual disability. Sources: Expert Review Green,ClinGen
Mode of inheritance for Region: ISCA-46743-Gain was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Rare multisystem ciliopathy Super panel v15.3 Arina Puzriakova Panel version 15.2 has been signed off on 2024-05-01
Hypotonic infant v29.2 Arina Puzriakova Panel version 29.1 has been signed off on 2024-05-01
Cystic renal disease v8.4 Eleanor Williams Panel version 8.3 has been signed off on 2024-05-01
Hereditary ataxia and cerebellar anomalies - childhood onset v15.3 Eleanor Williams Panel version 15.2 has been signed off on 2024-05-01
Sudden unexplained death or survivors of a cardiac event v19.74 Arina Puzriakova Panel version 19.73 has been signed off on 2024-05-01
Childhood onset leukodystrophy v19.3 Eleanor Williams Panel version 19.2 has been signed off on 2024-05-01
Unexplained death in infancy and sudden unexplained death in childhood v9.8 Arina Puzriakova Panel version 9.7 has been signed off on 2024-05-01
Cerebral malformation v11.3 Eleanor Williams Panel version 11.2 has been signed off on 2024-05-01
Other rare neuromuscular disorders v21.3 Eleanor Williams Panel version 21.2 has been signed off on 2024-05-01
Paediatric disorders v45.3 Arina Puzriakova Panel version 45.2 has been signed off on 2024-05-01
Short QT syndrome v3.12 Achchuthan Shanmugasundram Panel version 3.11 has been signed off on 2024-05-01
Progressive cardiac conduction disease v2.8 Achchuthan Shanmugasundram Panel version 2.7 has been signed off on 2024-05-01
Catecholaminergic polymorphic VT v4.6 Achchuthan Shanmugasundram Panel version 4.5 has been signed off on 2024-05-01
Hypertrophic cardiomyopathy v4.9 Achchuthan Shanmugasundram Panel version 4.8 has been signed off on 2024-05-01
Autoinflammatory disorders v2.1 Eleanor Williams Panel version 2.0 has been signed off on 2024-05-01
Autoinflammatory disorders v2.0 Eleanor Williams promoted panel to version 2.0
Brugada syndrome and cardiac sodium channel disease v3.10 Achchuthan Shanmugasundram Panel version 3.9 has been signed off on 2024-05-01
Unexplained young onset end-stage renal disease v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Differences in sex development v4.6 Achchuthan Shanmugasundram Panel version 4.5 has been signed off on 2024-05-01
Unexplained young onset end-stage renal disease v4.0 Eleanor Williams promoted panel to version 4.0
Arrhythmogenic right ventricular cardiomyopathy v3.11 Achchuthan Shanmugasundram Panel version 3.10 has been signed off on 2024-05-01
Cystic kidney disease v5.1 Eleanor Williams Panel version 5.0 has been signed off on 2024-05-01
Cystic kidney disease v5.0 Eleanor Williams promoted panel to version 5.0
Arthrogryposis v6.1 Achchuthan Shanmugasundram Panel version 6.0 has been signed off on 2024-05-01
Arthrogryposis v6.0 Achchuthan Shanmugasundram promoted panel to version 6.0
Retinal disorders v5.1 Eleanor Williams Panel version 5.0 has been signed off on 2024-05-01
Retinal disorders v5.0 Eleanor Williams promoted panel to version 5.0
Distal myopathies v4.1 Arina Puzriakova Panel version 4.0 has been signed off on 2024-05-01
Distal myopathies v4.0 Arina Puzriakova promoted panel to version 4.0
Severe microcephaly v5.1 Achchuthan Shanmugasundram Panel version 5.0 has been signed off on 2024-05-01
Malformations of cortical development v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Malformations of cortical development v5.0 Arina Puzriakova promoted panel to version 5.0
Ophthalmological ciliopathies v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Rhabdomyolysis and metabolic muscle disorders v4.1 Arina Puzriakova Panel version 4.0 has been signed off on 2024-05-01
Severe microcephaly v5.0 Achchuthan Shanmugasundram promoted panel to version 5.0
Rhabdomyolysis and metabolic muscle disorders v4.0 Arina Puzriakova promoted panel to version 4.0
Neurological ciliopathies v4.1 Achchuthan Shanmugasundram Panel version 4.0 has been signed off on 2024-05-01
Rare syndromic craniosynostosis or isolated multisuture synostosis v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Rare syndromic craniosynostosis or isolated multisuture synostosis v5.0 Arina Puzriakova promoted panel to version 5.0
Ophthalmological ciliopathies v4.0 Eleanor Williams promoted panel to version 4.0
Skeletal ciliopathies v4.1 Arina Puzriakova Panel version 4.0 has been signed off on 2024-05-01
Neurological ciliopathies v4.0 Achchuthan Shanmugasundram promoted panel to version 4.0
Neurological segmental overgrowth v2.13 Ivone Leong Panel version 2.12 has been signed off on 2024-05-01
Congenital myaesthenic syndrome v4.6 Ivone Leong Panel version 4.5 has been signed off on 2024-05-01
Ataxia and cerebellar anomalies - narrow panel v5.1 Achchuthan Shanmugasundram Panel version 5.0 has been signed off on 2024-05-01
Childhood onset dystonia, chorea or related movement disorder v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Ataxia and cerebellar anomalies - narrow panel v5.0 Achchuthan Shanmugasundram promoted panel to version 5.0
Skeletal ciliopathies v4.0 Arina Puzriakova promoted panel to version 4.0
Limb disorders v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
White matter disorders and cerebral calcification - narrow panel v4.1 Achchuthan Shanmugasundram Panel version 4.0 has been signed off on 2024-05-01
Childhood onset dystonia, chorea or related movement disorder v4.0 Eleanor Williams promoted panel to version 4.0
White matter disorders and cerebral calcification - narrow panel v4.0 Achchuthan Shanmugasundram promoted panel to version 4.0
DDG2P v4.1 Achchuthan Shanmugasundram Panel version 4.0 has been signed off on 2024-05-01
Hereditary neuropathy or pain disorder v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Limb disorders v5.0 Arina Puzriakova promoted panel to version 5.0
Hereditary neuropathy or pain disorder v4.0 Eleanor Williams promoted panel to version 4.0
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v4.33 Ivone Leong Panel version 4.32 has been signed off on 2024-05-01
DDG2P v4.0 Achchuthan Shanmugasundram promoted panel to version 4.0
Paediatric motor neuronopathies v3.7 Ivone Leong Panel version 3.6 has been signed off on 2024-05-01
Adult onset leukodystrophy v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Paediatric disorders - additional genes v4.1 Achchuthan Shanmugasundram Panel version 4.0 has been signed off on 2024-05-01
Adult onset leukodystrophy v4.0 Eleanor Williams promoted panel to version 4.0
Mitochondrial disorders v6.1 Arina Puzriakova Panel version 6.0 has been signed off on 2024-05-01
Familial hypoparathyroidism v2.15 Ivone Leong Panel version 2.14 has been signed off on 2024-05-01
Paediatric disorders - additional genes v4.0 Achchuthan Shanmugasundram promoted panel to version 4.0
Skeletal dysplasia v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Skeletal dysplasia v5.0 Arina Puzriakova promoted panel to version 5.0
Possible mitochondrial disorder - nuclear genes v3.106 Ivone Leong Panel version 3.105 has been signed off on 2024-05-01
Clefting v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Paediatric or syndromic cardiomyopathy v4.1 Achchuthan Shanmugasundram Panel version 4.0 has been signed off on 2024-05-01
Childhood onset hereditary spastic paraplegia v5.1 Eleanor Williams Panel version 5.0 has been signed off on 2024-05-01
Mitochondrial disorder with complex IV deficiency v3.21 Ivone Leong Panel version 3.20 has been signed off on 2024-05-01
Clefting v5.0 Arina Puzriakova promoted panel to version 5.0
Childhood onset hereditary spastic paraplegia v5.0 Eleanor Williams promoted panel to version 5.0
Respiratory ciliopathies including non-CF bronchiectasis v3.11 Ivone Leong Panel version 3.10 has been signed off on 2024-05-01
Adult onset hereditary spastic paraplegia v4.1 Eleanor Williams Panel version 4.0 has been signed off on 2024-05-01
Adult onset hereditary spastic paraplegia v4.0 Eleanor Williams promoted panel to version 4.0
Laterality disorders and isomerism v3.10 Ivone Leong Panel version 3.9 has been signed off on 2024-05-01
Mitochondrial disorders v6.0 Arina Puzriakova promoted panel to version 6.0
Paediatric or syndromic cardiomyopathy v4.0 Achchuthan Shanmugasundram promoted panel to version 4.0
Mitochondrial disorders v5.0 Arina Puzriakova promoted panel to version 5.0
Renal ciliopathies v3.6 Ivone Leong Panel version 3.5 has been signed off on 2024-05-01
Fetal anomalies v4.1 Arina Puzriakova Panel version 4.0 has been signed off on 2024-05-01
Early onset or syndromic epilepsy v5.1 Achchuthan Shanmugasundram Panel version 5.0 has been signed off on 2024-05-01
Fetal anomalies v4.0 Arina Puzriakova promoted panel to version 4.0
Holoprosencephaly - NOT chromosomal v4.5 Ivone Leong Panel version 4.4 has been signed off on 2024-05-01
Adult onset neurodegenerative disorder v5.1 Eleanor Williams Panel version 5.0 has been signed off on 2024-05-01
Adult onset neurodegenerative disorder v5.0 Eleanor Williams promoted panel to version 5.0
Early onset or syndromic epilepsy v5.0 Achchuthan Shanmugasundram promoted panel to version 5.0
Long QT syndrome v3.8 Ivone Leong Panel version 3.7 has been signed off on 2024-05-01
Hereditary ataxia with onset in adulthood v5.1 Eleanor Williams Panel version 5.0 has been signed off on 2024-05-01
Likely inborn error of metabolism v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Primary immunodeficiency or monogenic inflammatory bowel disease v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Dilated and arrhythmogenic cardiomyopathy v2.25 Ivone Leong Panel version 2.23 has been signed off on 2024-05-01
Hereditary ataxia with onset in adulthood v5.0 Eleanor Williams promoted panel to version 5.0
Primary immunodeficiency or monogenic inflammatory bowel disease v5.0 Arina Puzriakova promoted panel to version 5.0
Intellectual disability v6.1 Achchuthan Shanmugasundram Panel version 6.0 has been signed off on 2024-05-01
Monogenic hearing loss v4.40 Ivone Leong Panel version 4.39 has been signed off on 2024-05-01
Likely inborn error of metabolism v5.0 Arina Puzriakova promoted panel to version 5.0
Confirmed Fanconi anaemia or Bloom syndrome v2.6 Ivone Leong Panel version 2.5 has been signed off on 2024-05-01
Congenital disorders of glycosylation v5.1 Arina Puzriakova Panel version 5.0 has been signed off on 2024-05-01
Intellectual disability v6.0 Achchuthan Shanmugasundram promoted panel to version 6.0
Congenital disorders of glycosylation v5.0 Arina Puzriakova promoted panel to version 5.0
Dilated and arrhythmogenic cardiomyopathy v2.24 Ivone Leong Panel version 2.23 has been signed off on 2024-02-01
Paediatric disorders v35.1834 Achchuthan Shanmugasundram Changed child panels to: Intellectual disability; Early onset or syndromic epilepsy; Likely inborn error of metabolism - targeted testing not possible; Clefting; Skeletal dysplasia; Monogenic hearing loss; Limb disorders; DDG2P; Skeletal ciliopathies; Neurological ciliopathies; Paediatric disorders - additional genes; Ophthalmological ciliopathies; Renal ciliopathies
Unexplained death in infancy and sudden unexplained death in childhood v6.430 Eleanor Williams Changed child panels to: Early onset or syndromic epilepsy; Likely inborn error of metabolism - targeted testing not possible; Hypertrophic cardiomyopathy; Catecholaminergic polymorphic VT; Paediatric or syndromic cardiomyopathy; Short QT syndrome; Arrhythmogenic right ventricular cardiomyopathy; Brugada syndrome and cardiac sodium channel disease; Long QT syndrome; Dilated and arrhythmogenic cardiomyopathy; Progressive cardiac conduction disease
Confirmed Fanconi anaemia or Bloom syndrome v2.5 Ivone Leong List of related panels changed from R229; R258 to R229; R258; Confirmed Fanconi anaemia or Bloom syndrome - mutation testing; Cytopenia - Fanconi breakage testing indicated
Differences in sex development v4.5 Ivone Leong Panel name changed from Disorders of sex development to Differences in sex development
List of related panels changed from R146 to R146; Disorders of sex development
Intellectual disability v5.558 Arina Puzriakova Panel name changed from Intellectual disability - microarray and sequencing to Intellectual disability
List of related panels changed from Coarse facial features including Coffin-Siris-like disorders; ID; Moderate; severe or profound intellectual disability; Schizophrenia plus additional features; Intellectual disability - microarray; fragile X and sequencing; Intellectual disability; R29 to Coarse facial features including Coffin-Siris-like disorders; ID; Moderate; severe or profound intellectual disability; Schizophrenia plus additional features; Intellectual disability - microarray; fragile X and sequencing; Intellectual disability - microarray and sequencing; R29
Intellectual disability v5.557 DIP2B Dmitrijs Rots reviewed gene: DIP2B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Intellectual disability v5.557 ADGRL1 Dmitrijs Rots gene: ADGRL1 was added
gene: ADGRL1 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: ADGRL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ADGRL1 were set to PubMed: 35907405
Phenotypes for gene: ADGRL1 were set to Developmental delay, behavioral abnormalities, and neuropsychiatric disorders
Review for gene: ADGRL1 was set to GREEN
Added comment: More than 10 cases described in PubMed: 35907405
Sources: Literature
Hypertrophic cardiomyopathy v4.7 SVIL Dmitrijs Rots gene: SVIL was added
gene: SVIL was added to Hypertrophic cardiomyopathy. Sources: Literature
Mode of inheritance for gene: SVIL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SVIL were set to PMID: 36778260
Phenotypes for gene: SVIL were set to HCM
Review for gene: SVIL was set to AMBER
Added comment: In the novel paper described:"the excess burden is even greater at 15.3-fold (95% CI: 5.7-41.3; P:7x10−7) when restricting the analysis to high confidence LoF variants affecting the predominant SVIL transcript in LV (ENST00000375400) (Supplementary Table 6b). In one family, the SVIL LoF variant (p.(Gln255*)) was carried by two cousins with HCM (parents deceased), providing some evidence of co-segregation. Taken together, these data support SVIL as a novel HCM disease gene."
Strong statistical evidence + one family segregating.
Sources: Literature
Familial non syndromic congenital heart disease v1.80 FLT4 Dmitrijs Rots edited their review of gene: FLT4: Added comment: Statistically proven 30582441 enrichment in multiple affected cases. Enough for green rating.; Changed phenotypes to: Congenital heart defect; Set current diagnostic: yes
Familial non syndromic congenital heart disease v1.80 FLT4 Dmitrijs Rots reviewed gene: FLT4: Rating: GREEN; Mode of pathogenicity: None; Publications: 30582441; Phenotypes: Congenital; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Thrombophilia with a likely monogenic cause v2.5 PLG Zornitza Stark reviewed gene: PLG: Rating: AMBER; Mode of pathogenicity: None; Publications: 35244080, 27976734; Phenotypes: Dysplasminogenemia, MIM# 217090; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Familial breast cancer v1.20 BARD1 Dmitrijs Rots edited their review of gene: BARD1: Added comment: PMID: 37592023 metaanlysis also reports significant association with breast cancer; Changed publications to: PMID: 37592023
Familial breast cancer v1.20 BARD1 Dmitrijs Rots reviewed gene: BARD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v5.31 SLC35A3 Hannah Knight reviewed gene: SLC35A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28777481, 24031089, 28328131, 33416188; Phenotypes: Arthrogryposis, impaired intellectual development, and seizures, 615553 (3), Autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v5.557 ZNFX1 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: ZNFX1.
Early onset or syndromic epilepsy v4.196 ZNFX1 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: ZNFX1.
Early onset or syndromic epilepsy v4.196 YIF1B Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: YIF1B.
Severe microcephaly v4.88 YIF1B Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: YIF1B.
Early onset or syndromic epilepsy v4.196 TRIT1 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: TRIT1.
Ataxia and cerebellar anomalies - narrow panel v4.64 SVBP Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: SVBP.
Intellectual disability v5.557 RNPC3 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: RNPC3.
Mitochondrial disorders v4.169 PITRM1 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: PITRM1.
Likely inborn error of metabolism v4.137 PITRM1 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: PITRM1.
Intellectual disability v5.557 FILIP1 Achchuthan Shanmugasundram Tag gene-checked was removed from gene: FILIP1.
Arthrogryposis v5.31 FILIP1 Achchuthan Shanmugasundram Tag gene-checked was removed from gene: FILIP1.
Intellectual disability v5.557 OTUD7A Achchuthan Shanmugasundram Tag gene-checked was removed from gene: OTUD7A.
Early onset or syndromic epilepsy v4.196 OTUD7A Achchuthan Shanmugasundram Tag gene-checked was removed from gene: OTUD7A.
Hypertrophic cardiomyopathy v4.7 ALPK3 Dmitrijs Rots commented on gene: ALPK3: As described by Luis Lopes, should be BOTH monoallelic and biallelic on this panel.
Intellectual disability v5.557 CEP295 Achchuthan Shanmugasundram Phenotypes for gene: CEP295 were changed from Seckel syndrome 11, OMIM # 620767 to Seckel syndrome 11, OMIM:620767
Intellectual disability v5.556 CEP295 Achchuthan Shanmugasundram Classified gene: CEP295 as Amber List (moderate evidence)
Intellectual disability v5.556 CEP295 Achchuthan Shanmugasundram Gene: cep295 has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.555 CEP295 Achchuthan Shanmugasundram reviewed gene: CEP295: Rating: AMBER; Mode of pathogenicity: None; Publications: 38154379; Phenotypes: Seckel syndrome 11, OMIM:620767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v5.555 DOCK4 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: DOCK4.
Intellectual disability v5.555 DOCK4 Achchuthan Shanmugasundram Classified gene: DOCK4 as Amber List (moderate evidence)
Intellectual disability v5.555 DOCK4 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Zornitza Stark, PMID:38526744 reported seven unrelated individuals with heterozygous variants and with developmental delay or intellectual disability, of which four had ID. Three of them with ID had heterozygous variants, while one had compound heterozygous variants. There is also some functional evidence available.

Hence, this gene can be promoted to green rating in the next GMS review.
Intellectual disability v5.555 DOCK4 Achchuthan Shanmugasundram Gene: dock4 has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.554 DOCK4 Achchuthan Shanmugasundram Phenotypes for gene: DOCK4 were changed from neuronevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071 to neuronevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071
Intellectual disability v5.554 DOCK4 Achchuthan Shanmugasundram Phenotypes for gene: DOCK4 were changed from DOCK4-related neurodevelopmental disorder (MONDO:0060490) to neuronevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071
Intellectual disability v5.553 DOCK4 Achchuthan Shanmugasundram reviewed gene: DOCK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 38526744; Phenotypes: neuronevelopmental disorder, MONDO:0700092, intellectual disability, MONDO:0001071; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v5.553 GTF3C5 Achchuthan Shanmugasundram Publications for gene: GTF3C5 were set to 38520561; 35503477
Intellectual disability v5.552 GTF3C5 Achchuthan Shanmugasundram changed review comment from: Comment on list classification: As reviewed by Zornitza Stark, PMID:35503477 reported a proband with profound developmental delay and PMID:38520561 reported three families with syndromic intellectual disability (ID was mild in one family). There is also functional evidence and evidence from zebrafish model in support of the disease association.

Hence, the gene can be promoted to green rating in the next GMS review.; to: Comment on list classification: As reviewed by Zornitza Stark, PMID:35503477 reported a proband with profound developmental delay and PMID:38520561 reported three families with syndromic intellectual disability (ID was mild in one family). There is also functional evidence and evidence from zebrafish model in support of the disease association.

Hence, this gene can be promoted to green rating in the next GMS review.
Intellectual disability v5.552 GTF3C5 Achchuthan Shanmugasundram edited their review of gene: GTF3C5: Changed publications to: 35503477, 38520561
Intellectual disability v5.552 GTF3C5 Achchuthan Shanmugasundram Classified gene: GTF3C5 as Amber List (moderate evidence)
Intellectual disability v5.552 GTF3C5 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Zornitza Stark, PMID:35503477 reported a proband with profound developmental delay and PMID:38520561 reported three families with syndromic intellectual disability (ID was mild in one family). There is also functional evidence and evidence from zebrafish model in support of the disease association.

Hence, the gene can be promoted to green rating in the next GMS review.
Intellectual disability v5.552 GTF3C5 Achchuthan Shanmugasundram Gene: gtf3c5 has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.551 GTF3C5 Achchuthan Shanmugasundram Phenotypes for gene: GTF3C5 were changed from neurodevelopmental disorder MONDO:0700092, GTF3C5-related to neurodevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071
Intellectual disability v5.550 GTF3C5 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: GTF3C5.
Intellectual disability v5.550 GTF3C5 Achchuthan Shanmugasundram reviewed gene: GTF3C5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: neurodevelopmental disorder, MONDO:0700092, intellectual disability, MONDO:0001071; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Skeletal ciliopathies v3.23 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Childhood onset dystonia, chorea or related movement disorder v3.78 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Neurological ciliopathies v3.20 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Ophthalmological ciliopathies v3.7 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Intellectual disability v5.550 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Rare multisystem ciliopathy disorders v1.172 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
DDG2P v3.90 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome to Stromme syndrome, OMIM:243605
Fetal anomalies v3.169 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605 to Stromme syndrome, OMIM:243605
Unexplained young onset end-stage renal disease v3.42 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome to Stromme syndrome, OMIM:243605; Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
CAKUT v1.177 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Stromme syndrome, 243605; bilateral renal hypoplasia; Duodenal atresia; Hydronephrosis to Stromme syndrome, OMIM:243605
Limb disorders v4.23 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from Polydactyly; Stromme syndrome 243605 to Stromme syndrome, OMIM:243605
Severe microcephaly v4.88 CENPF Arina Puzriakova Phenotypes for gene: CENPF were changed from MPD; microcephalic primordial dwarfism; Stromme syndrome, 243605; Microcephaly to Stromme syndrome, OMIM:243605; Microcephalic primordial dwarfism
Intellectual disability v5.549 GMNN Arina Puzriakova Phenotypes for gene: GMNN were changed from Meier-Gorlin syndrome 6, 616835 to Meier-Gorlin syndrome 6, OMIM:616835
Clefting v4.111 GMNN Arina Puzriakova Phenotypes for gene: GMNN were changed from Meier-Gorlin syndrome 6, 616835 to Meier-Gorlin syndrome 6, OMIM:616835
Severe microcephaly v4.87 GMNN Arina Puzriakova Phenotypes for gene: GMNN were changed from MPD; microcephalic primordial dwarfism; Meier-Gorlin syndrome 6, 616835; MGORS6; primordial dwarfism to Meier-Gorlin syndrome 6, OMIM:616835; Microcephalic primordial dwarfism
Intellectual disability v5.548 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747; INSULIN-LIKE GROWTH FACTOR I DEFICIENCY (IGF1 DEFICIENCY) to Insulin-like growth factor I deficiency, OMIM:608747
Monogenic hearing loss v4.39 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from Growth retardation with deafness and mental retardation due to IGF1 deficiency,608747; GrowthretardationwithdeafnessandmentalretardationduetoIGF1deficiency,608747 to Insulin-like growth factor I deficiency, OMIM:608747
DDG2P v3.89 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from INSULIN-LIKE GROWTH FACTOR I DEFICIENCY 608747 to Insulin-like growth factor I deficiency, OMIM:608747
Fetal anomalies v3.168 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from INSULIN-LIKE GROWTH FACTOR I DEFICIENCY to Insulin-like growth factor I deficiency, OMIM:608747
IUGR and IGF abnormalities v1.69 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747; Insulin-Like Growth Factor I Deficiency to Insulin-like growth factor I deficiency, OMIM:608747
Silver Russell syndrome v1.13 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from Growth retardation with deafness and mental retardation due to IGF1 deficiency 608747 to Insulin-like growth factor I deficiency, OMIM:608747
Severe microcephaly v4.86 IGF1 Arina Puzriakova Phenotypes for gene: IGF1 were changed from Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747; MPD; microcephalic primordial dwarfism to Insulin-like growth factor I deficiency, OMIM:608747; Microcephalic primordial dwarfism
Intellectual disability v5.547 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from LIG4 syndrome, OMIM:606593 to LIG4 syndrome, OMIM:606593
Haematological malignancies cancer susceptibility v4.5 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from Class: miscellaneous; Ligase IV syndrome; Lymphoma; ALL to LIG4 syndrome, OMIM:606593; Ligase IV syndrome; Lymphoma; ALL
Intellectual disability v5.547 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from LIG4 syndrome, 606593{Multiple myeloma, resistance to}, 254500Severe combined immunodeficiency with sensitivity to ionizing radiation, 602450; LIG4 SYNDROME to LIG4 syndrome, OMIM:606593
Fetal anomalies v3.167 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from SEVERE COMBINED IMMUNODEFICIENCY AUTOSOMAL RECESSIVE T-CELL-NEGATIVE/B-CELL-NEGATIVE/NK-CELL-POSITIVE WITH SENSITIVITY TO IONIZING RADIATION; LIG4 SYNDROME to LIG4 syndrome, OMIM:606593
Cytopenia - NOT Fanconi anaemia v3.34 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from 606593 LIG4 syndrome to LIG4 syndrome, OMIM:606593
IUGR and IGF abnormalities v1.68 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from microcephaly, growth retardation, immunodeficiency, developmental delay to LIG4 syndrome, OMIM:606593; microcephaly, growth retardation, immunodeficiency, developmental delay
Haematological malignancies for rare disease v1.18 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from Class: miscellaneous; Ligase IV syndrome; Lymphoma; ALL to LIG4 syndrome, OMIM:606593; Class: miscellaneous; Ligase IV syndrome; Lymphoma; ALL
Infantile enterocolitis & monogenic inflammatory bowel disease v1.44 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from SCID; LIG4 syndrome 606593 to LIG4 syndrome, OMIM:606593
Severe microcephaly v4.85 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from MPD; microcephalic primordial dwarfism; LIG4 syndrome, 606593; microcephaly to LIG4 syndrome, OMIM:606593; Microcephalic primordial dwarfism
Intellectual disability v5.546 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from Meier-Gorlin syndrome 1, 224690; MEIER-GORLIN SYNDROME 1 to Meier-Gorlin syndrome 1, OMIM:224690
Skeletal dysplasia v4.65 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from Meier-Gorlin syndrome 1 224690; Meier-Gorlin syndrome 1 224690 to Meier-Gorlin syndrome 1, OMIM:224690
Fetal anomalies v3.166 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from MEIER-GORLIN SYNDROME 1 to Meier-Gorlin syndrome 1, OMIM:224690
Limb disorders v4.22 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from Meier-Gorlin syndrome 1 to Meier-Gorlin syndrome 1, OMIM:224690
Deafness and congenital structural abnormalities v1.27 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from Bilateral Microtia; 224690; Meier Gorlin EPS; causes microtia and syndromic features; Meier-Gorlin syndrome 1 to Meier-Gorlin syndrome 1, OMIM:224690; Bilateral Microtia
IUGR and IGF abnormalities v1.67 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from microtia, beaked nose, patellar aplasia/hypoplasia, mammary hypoplasia, micrognathia to Meier-Gorlin syndrome 1, OMIM:224690; microtia, beaked nose, patellar aplasia/hypoplasia, mammary hypoplasia, micrognathia
Severe microcephaly v4.84 ORC1 Arina Puzriakova Phenotypes for gene: ORC1 were changed from MPD; microcephalic primordial dwarfism; Meier-Gorlin syndrome 1, 224690 to Meier-Gorlin syndrome 1, OMIM:224690; Microcephalic primordial dwarfism
Intellectual disability v5.545 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from Meier-Gorlin syndrome 2, 613800 to Meier-Gorlin syndrome 2, OMIM:613800
Fetal anomalies v3.165 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from MEIER-GORLIN SYNDROME 2 to Meier-Gorlin syndrome 2, OMIM:613800
Skeletal dysplasia v4.64 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from Meier-Gorlin syndrome 2 613800; Meier-Gorlin syndrome 2 613800 to Meier-Gorlin syndrome 2, OMIM:613800
Deafness and congenital structural abnormalities v1.26 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from Bilateral Microtia; 613800; Meier-Gorlin EPS; causes syndromic features to Meier-Gorlin syndrome 2, OMIM:613800; Bilateral Microtia
IUGR and IGF abnormalities v1.66 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia to Meier-Gorlin syndrome 2, OMIM:613800; micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia
Severe microcephaly v4.83 ORC4 Arina Puzriakova Phenotypes for gene: ORC4 were changed from MPD; microcephalic primordial dwarfism; Meier-Gorlin syndrome 2, 613800 to Meier-Gorlin syndrome 2, OMIM:613800; Microcephalic primordial dwarfism
Breast cancer pertinent cancer susceptibility v2.8 PTEN Dmitrijs Rots reviewed gene: PTEN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: PHTS; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v5.31 COASY Achchuthan Shanmugasundram Classified gene: COASY as Amber List (moderate evidence)
Arthrogryposis v5.31 COASY Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for promoting this gene to green rating in the next GMS review.
Arthrogryposis v5.31 COASY Achchuthan Shanmugasundram Gene: coasy has been classified as Amber List (Moderate Evidence).
Arthrogryposis v5.30 COASY Achchuthan Shanmugasundram Phenotypes for gene: COASY were changed from Pontocerebellar hypoplasia, type 12, OMIM:618266; pontocerebellar hypoplasia, type 12, MONDO:0032643 to Neurodegeneration with brain iron accumulation 6, OMIM:615643; Pontocerebellar hypoplasia, type 12, OMIM:618266; arthrogryposis, MONDO:0008779
Arthrogryposis v5.29 COASY Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: COASY.
Tag Q2_24_NHS_review tag was added to gene: COASY.
Arthrogryposis v5.29 COASY Achchuthan Shanmugasundram reviewed gene: COASY: Rating: GREEN; Mode of pathogenicity: None; Publications: 30089828, 35499143, 36495139; Phenotypes: Neurodegeneration with brain iron accumulation 6, OMIM:615643, Pontocerebellar hypoplasia, type 12, OMIM:618266, arthrogryposis, MONDO:0008779; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v5.29 PIP5K1C Achchuthan Shanmugasundram Phenotypes for gene: PIP5K1C were changed from Lethal congenital contractural syndrome 3 611369 to Lethal congenital contractural syndrome 3, OMIM:611369
Arthrogryposis v5.28 PIP5K1C Achchuthan Shanmugasundram Publications for gene: PIP5K1C were set to 17701898
Arthrogryposis v5.27 PIP5K1C Achchuthan Shanmugasundram Classified gene: PIP5K1C as Amber List (moderate evidence)
Arthrogryposis v5.27 PIP5K1C Achchuthan Shanmugasundram Added comment: Comment on list classification: As there are three unrelated cases with biallelic variants (two unrelated cases with the same homozygous variant and two foetuses from one family with compound heterozygous variants), this gene can be promoted to green rating in the next GMS update.
Arthrogryposis v5.27 PIP5K1C Achchuthan Shanmugasundram Gene: pip5k1c has been classified as Amber List (Moderate Evidence).
Arthrogryposis v5.26 PIP5K1C Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: PIP5K1C.
Tag Q2_24_NHS_review tag was added to gene: PIP5K1C.
Arthrogryposis v5.26 PIP5K1C Achchuthan Shanmugasundram reviewed gene: PIP5K1C: Rating: GREEN; Mode of pathogenicity: None; Publications: 17701898, 38491417; Phenotypes: Lethal congenital contractural syndrome 3, OMIM:611369; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v5.26 TRIP4 Achchuthan Shanmugasundram reviewed gene: TRIP4: Rating: AMBER; Mode of pathogenicity: None; Publications: 31794073; Phenotypes: Spinal muscular atrophy with congenital bone fractures 1, OMIM:616866, ?Muscular dystrophy, congenital, Davignon-Chauveau type, OMIM:617066; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v5.26 COASY Achchuthan Shanmugasundram Publications for gene: COASY were set to 11980892; 25778941; 24360804; 27021474; 28489334; 30089828; 36495139
Ectodermal dysplasia v3.29 TWIST2 Dmitrijs Rots gene: TWIST2 was added
gene: TWIST2 was added to Ectodermal dysplasia. Sources: Expert Review
Mode of inheritance for gene: TWIST2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TWIST2 were set to Focal facial dermal dysplasia 3, Setleis type
Review for gene: TWIST2 was set to GREEN
Added comment: Included as differential for ectodermal dysplasia
Sources: Expert Review
Arthrogryposis v5.25 SLC18A3 Achchuthan Shanmugasundram Classified gene: SLC18A3 as Amber List (moderate evidence)
Arthrogryposis v5.25 SLC18A3 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Hannah Knight, PMID:34943989 reports an additional patient with compound heterozygous variants in SLC18A3 gene and presenting with arthrogryposis congenital (AMC). Hence, there is sufficient evidence available for promoting this gene to green rating in the next GMS review.
Arthrogryposis v5.25 SLC18A3 Achchuthan Shanmugasundram Gene: slc18a3 has been classified as Amber List (Moderate Evidence).
Arthrogryposis v5.24 SLC18A3 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: SLC18A3.
Tag Q2_24_NHS_review tag was added to gene: SLC18A3.
Arthrogryposis v5.24 SLC18A3 Achchuthan Shanmugasundram edited their review of gene: SLC18A3: Changed phenotypes to: Myasthenic syndrome, congenital, 21, presynaptic, OMIM:617239, arthrogryposis, MONDO:0008779
Arthrogryposis v5.24 SLC18A3 Achchuthan Shanmugasundram Phenotypes for gene: SLC18A3 were changed from Myasthenic syndrome, congenital, 21, presynaptic, 617239; arthrogryposis to Myasthenic syndrome, congenital, 21, presynaptic, OMIM:617239; arthrogryposis, MONDO:0008779
Arthrogryposis v5.23 SLC18A3 Achchuthan Shanmugasundram Publications for gene: SLC18A3 were set to 28188302; 27590285; 31059209
Arthrogryposis v5.22 SLC18A3 Achchuthan Shanmugasundram reviewed gene: SLC18A3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Skeletal dysplasia v4.63 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from Meier-Gorlin syndrome 3 613803; Meier-Gorlin syndrome 3 613803 to Meier-Gorlin syndrome 3, OMIM:613803
Intellectual disability v5.544 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from Meier-Gorlin syndrome 3, 613803 to Meier-Gorlin syndrome 3, OMIM:613803
Fetal anomalies v3.164 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from MEIER-GORLIN SYNDROME 3 to Meier-Gorlin syndrome 3, OMIM:613803
Deafness and congenital structural abnormalities v1.25 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from Bilateral Microtia; 613803; Meier-Gorlin EPS; causes syndromic features; Meier-Gorlin syndrome 3 to Meier-Gorlin syndrome 3, OMIM:613803; Bilateral Microtia
IUGR and IGF abnormalities v1.65 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia to Meier-Gorlin syndrome 3, OMIM:613803; micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia
Severe microcephaly v4.82 ORC6 Arina Puzriakova Phenotypes for gene: ORC6 were changed from MPD; microcephalic primordial dwarfism; Meier-Gorlin syndrome 3, 613803 to Meier-Gorlin syndrome 3, OMIM:613803; Microcephalic primordial dwarfism
Insulin resistance (including lipodystrophy) v1.17 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II 210720; Osteodysplastic Primordial Dwarfism of Majewski Tyoe 2; Severe Insulin Resistance to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720; Insulin resistance, HP:0000855
IUGR and IGF abnormalities v1.64 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from Seckel syndrome, MOPD type II - growth restrction, microcephaly, prominent nose, micrognathia, squeaky voice, insulin resistance to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
Limb disorders v4.21 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II 210720 to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
Skeletal dysplasia v4.62 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II 210720 to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
DDG2P v3.88 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II 210720 to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
Fetal anomalies v3.163 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
Intellectual disability v5.543 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II, 210720 -3; MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720
Severe microcephaly v4.81 PCNT Arina Puzriakova Phenotypes for gene: PCNT were changed from MPD; microcephalic primordial dwarfism; Microcephalic Osteodysplastic Primordial Dwarfism; Microcephalic osteodysplastic primordial dwarfism, type II, 210720 to Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720; Microcephalic primordial dwarfism
Retinal disorders v4.90 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Lowry-Wood syndrome, OMIM:226960; Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710; Roifman syndrome, OMIM:616651 to Lowry-Wood syndrome, OMIM:226960; Roifman syndrome, OMIM:616651
Intellectual disability v5.542 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Gene2Phenotype confirmed gene with ID HPO to Lowry-Wood syndrome, OMIM:226960; Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710; Roifman syndrome, OMIM:616651
Early onset or syndromic epilepsy v4.196 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Microcephalic osteodysplastic primordial dwarfism, type I 210710 to Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710
Fetal anomalies v3.162 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I to Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710
Cytopenia - NOT Fanconi anaemia v3.33 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Roifman syndrome, 616651; Microcephalic osteodysplastic primordial dwarfism, type I, 210710 to Roifman syndrome, OMIM:616651
Bleeding and platelet disorders v3.10 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Microcephalic osteodysplastic primordial dwarfism, type I / Roifman syndrome to Roifman syndrome, OMIM:616651
Inherited bleeding disorders v1.178 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Platelet disorder; Roifman Syndrome with thrombocytopenia and Primary immunodeficiency to Roifman syndrome, OMIM:616651; Roifman Syndrome with thrombocytopenia and Primary immunodeficiency
Skeletal dysplasia v4.61 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Roifman syndrome 616651; Microcephalic osteodysplastic primordial dwarfism, type I 210710 to Lowry-Wood syndrome, OMIM:226960; Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710; Roifman syndrome, OMIM:616651
Limb disorders v4.20 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Microcephalic osteodysplastic primordial dwarfism, type I 210710; Roifman syndrome 616651 to Lowry-Wood syndrome, OMIM:226960; Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710; Roifman syndrome, OMIM:616651
Primary immunodeficiency or monogenic inflammatory bowel disease v4.202 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly, short stature; Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly; Combined immunodeficiencies with associated or syndromic features to Roifman syndrome, OMIM:616651; Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly
COVID-19 research v1.142 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly; Combined immunodeficiencies with associated or syndromic features; Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly, short stature to Roifman syndrome, OMIM:616651; Recurrent bacterial infections, lymphadenopathy, Spondyloepiphyseal dysplasia, extreme intrauterine growth retardation, retinal dystrophy, facial dysmorphism, may present with microcephaly
Severe microcephaly v4.80 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Microcephalic osteodysplastic primordial dwarfism, type I; Microcephalic osteodysplastic primordial dwarfism, type I, 210710; MPD; microcephalic primordial dwarfism to Microcephalic osteodysplastic primordial dwarfism, type I, OMIM:210710; Lowry-Wood syndrome, OMIM:226960; Microcephalic primordial dwarfism
Intellectual disability v5.541 TRAIP Arina Puzriakova Phenotypes for gene: TRAIP were changed from Seckel syndrome 9, 616777 to Seckel syndrome 9, OMIM:616777
Cerebral vascular malformations v3.16 TRAIP Arina Puzriakova Phenotypes for gene: TRAIP were changed from Seckel syndrome 9 616777 to Seckel syndrome 9, OMIM:616777
Fetal anomalies v3.161 TRAIP Arina Puzriakova Phenotypes for gene: TRAIP were changed from Seckel syndrome 9 to Seckel syndrome 9, OMIM:616777
Severe microcephaly v4.79 TRAIP Arina Puzriakova Phenotypes for gene: TRAIP were changed from MPD; microcephalic primordial dwarfism; Seckel syndrome 9, 616777; Microcephaly to Seckel syndrome 9, OMIM:616777; Microcephalic primordial dwarfism
Mitochondrial disorders v4.169 XRCC4 Arina Puzriakova Mode of inheritance for gene: XRCC4 was changed from to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v4.169 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from Short stature, microcephaly, and endocrine dysfunction 616541 to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541
Fetal anomalies v3.160 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from PRIMORDIAL DWARFISM to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541
Skeletal dysplasia v4.60 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from Short stature, microcephaly, and endocrine dysfunction 616541 to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541
Intellectual disability v5.540 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from PRIMORDIAL DWARFISM to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541
IUGR and IGF abnormalities v1.63 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from short stature, microcephaly, hypothyroidism, diabetes mellitus, progressive ataxia, hypergonadotrophic hypogonadism to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541; Short stature, microcephaly, hypothyroidism, diabetes mellitus, progressive ataxia, hypergonadotrophic hypogonadism
Severe microcephaly v4.78 XRCC4 Arina Puzriakova Phenotypes for gene: XRCC4 were changed from MPD; microcephalic primordial dwarfism; Short stature, microcephaly, and endocrine dysfunction, 616541 to Short stature, microcephaly, and endocrine dysfunction, OMIM:616541; Microcephalic primordial dwarfism
Severe microcephaly v4.77 ATRIP Arina Puzriakova Publications for gene: ATRIP were set to
Severe microcephaly v4.76 ATRIP Arina Puzriakova Mode of inheritance for gene: ATRIP was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe microcephaly v4.75 ATRIP Arina Puzriakova Phenotypes for gene: ATRIP were changed from MPD; microcephalic primordial dwarfism; severe microcephaly (-10 SD), micrognathia, dental crowding, small earlobes, delayed bone age, and symmetric dwarfism to Microcephalic primordial dwarfism; Severe microcephaly (-10 SD), micrognathia, dental crowding, small earlobes, delayed bone age, and symmetric dwarfism
Intellectual disability v5.539 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from MEIER-GORLIN SYNDROME 5 to Meier-Gorlin syndrome 5, OMIM:613805
Skeletal dysplasia v4.59 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from Meier-Gorlin syndrome 5 613805 to Meier-Gorlin syndrome 5, OMIM:613805
Fetal anomalies v3.159 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from MEIER-GORLIN SYNDROME 5 to Meier-Gorlin syndrome 5, OMIM:613805
Deafness and congenital structural abnormalities v1.24 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from Bilateral Microtia; 613805; Meier-Gorlin syndrome 5, 613805; Neurology panel; Bilateral Microtia, 613805; Causes Meier-Gorlin EPS; syndromic features to Meier-Gorlin syndrome 5, OMIM:613805; Bilateral Microtia
IUGR and IGF abnormalities v1.62 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from patellar hypoplasia/aplasia, microtia, meier-gorlin syndrome, mammary hypoplasia to Meier-Gorlin syndrome 5, OMIM:613805; patellar hypoplasia/aplasia, microtia, meier-gorlin syndrome, mammary hypoplasia
Severe microcephaly v4.74 CDC6 Arina Puzriakova Phenotypes for gene: CDC6 were changed from MPD; microcephalic primordial dwarfism; ?Meier-Gorlin syndrome 5, 613805 to Meier-Gorlin syndrome 5, OMIM:613805; Microcephalic primordial dwarfism
Severe microcephaly v4.73 CENPE Arina Puzriakova Phenotypes for gene: CENPE were changed from ?Microcephaly 13, primary, autosomal recessive, 616051; MPD; microcephalic primordial dwarfism to ?Microcephaly 13, primary, autosomal recessive, OMIM:616051; Microcephalic primordial dwarfism
Intellectual disability v5.538 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from MEIER-GORLIN SYNDROME 4 to Meier-Gorlin syndrome 4, OMIM:613804
Skeletal dysplasia v4.58 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from Meier-Gorlin syndrome 4 613804 to Meier-Gorlin syndrome 4, OMIM:613804
Fetal anomalies v3.158 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from MEIER-GORLIN SYNDROME 4 to Meier-Gorlin syndrome 4, OMIM:613804
Deafness and congenital structural abnormalities v1.23 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from Bilateral Microtia; 613804; Meier-Gorlin syndrome 4, 613804; Causes Meier-Gorlin EPS; syndromic features; Short stature, small head size, the ears may be low-set or rotated backward (+/-microtia). Additional features can include a small mouth (microstomia), an underdeveloped lower jaw (micrognathia), full lips, and a narrow nose with a high nasal bridge to Meier-Gorlin syndrome 4, OMIM:613804; Short stature, small head size, the ears may be low-set or rotated backward (+/-microtia). Additional features can include a small mouth (microstomia), an underdeveloped lower jaw (micrognathia), full lips, and a narrow nose with a high nasal bridge
IUGR and IGF abnormalities v1.61 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from micrognathia, microtia, patellar hypoplasia/aplasia, mammary hypoplasia to Meier-Gorlin syndrome 4, OMIM:613804; micrognathia, microtia, patellar hypoplasia/aplasia, mammary hypoplasia
Severe microcephaly v4.72 CDT1 Arina Puzriakova Phenotypes for gene: CDT1 were changed from MPD; microcephalic primordial dwarfism; Meier-Gorlin syndrome 4, 613804 to Meier-Gorlin syndrome 4, OMIM:613804; Microcephalic primordial dwarfism
Monogenic diabetes v2.58 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Bloom syndrome to Bloom syndrome, OMIM:210900
Pigmentary skin disorders v3.12 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Bloom syndrome to Bloom syndrome, OMIM:210900
Primary ovarian insufficiency v1.68 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Bloom syndrome 210900 to Bloom syndrome, OMIM:210900
IUGR and IGF abnormalities v1.60 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Bloom syndrome, 210900 to Bloom syndrome, OMIM:210900
Haematological malignancies for rare disease v1.17 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Class: BM failure syndrome (typ AR); Bloom syndrome; leukaemia; lymphoma; skin squamous cell; other tumour types; Lymphoma; ALL; MDS; AML; Leukaemia; Carcinomas to Bloom syndrome, OMIM:210900; Class: BM failure syndrome (typ AR); Bloom syndrome; leukaemia; lymphoma; skin squamous cell; other tumour types; Lymphoma; ALL; MDS; AML; Leukaemia; Carcinomas
Severe microcephaly v4.71 BLM Arina Puzriakova Phenotypes for gene: BLM were changed from Bloom syndrome, OMIM:210900 to Bloom syndrome, OMIM:210900; Microcephalic primordial dwarfism
Hereditary haemorrhagic telangiectasia v3.6 ATR Arina Puzriakova Phenotypes for gene: ATR were changed from Cutaneous telangiectasia and cancer syndrome, familial, 614564 (biallelic) to ?Cutaneous telangiectasia and cancer syndrome, familial, OMIM:614564
Intellectual disability v5.537 ATR Arina Puzriakova Phenotypes for gene: ATR were changed from Seckel syndrome 1, 210600Cutaneous telangiectasia and cancer syndrome, familial, 614564; SECKEL SYNDROME TYPE 1 (SCKL1) to Seckel syndrome 1, OMIM:210600
Clefting v4.110 ATR Arina Puzriakova Phenotypes for gene: ATR were changed from SECKEL SYNDROME 1; SCKL1 to Seckel syndrome 1, OMIM:210600
Clefting v4.110 ATR Arina Puzriakova Mode of inheritance for gene: ATR was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe microcephaly v4.70 ATR Arina Puzriakova Publications for gene: ATR were set to
Severe microcephaly v4.69 ATR Arina Puzriakova Phenotypes for gene: ATR were changed from MPD; microcephalic primordial dwarfism; Seckel syndrome 1, 210600; MICROCEPHALIC PRIMORDIAL DWARFISM I to Seckel syndrome 1, OMIM:210600; Microcephalic primordial dwarfism
Intellectual disability v5.536 FEM1B Zornitza Stark edited their review of gene: FEM1B: Added comment: Five individuals reported now with same recurrent missense variant, NM_015322.5:c.377G>A NP_056137.1:p.(Arg126Gln). Affected individuals shared a severe neurodevelopmental disorder with behavioral phenotypes and a variable set of malformations, including brain anomalies, clubfeet, skeletal abnormalities, and facial dysmorphism. Overexpression of the the FEM1BR126Q variant but not FEM1B wild-type protein, during mouse brain development, resulted in delayed neuronal migration of the target cells.; Changed rating: GREEN; Changed publications to: 31036916, 38465576; Changed phenotypes to: Syndromic disease MONDO:0002254, FEM1B-related
Fetal anomalies v3.157 USP14 Zornitza Stark gene: USP14 was added
gene: USP14 was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: USP14 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: USP14 were set to 38469793
Phenotypes for gene: USP14 were set to Syndromic disease MONDO:0002254, USP14-related
Review for gene: USP14 was set to AMBER
Added comment: PMID 38469793: biallelic USP14 variants in four individuals from three unrelated families: one fetus, a newborn with a syndromic NDD, and two siblings affected by a progressive neurological disease. Specifically, the two siblings from the latter family carried two compound heterozygous variants c.8T>C p.(Leu3Pro) and c.988C>T p.(Arg330*), while the fetus had a homozygous frameshift c.899_902del p.(Lys300Serfs*24) variant and the newborn patient harbored a homozygous frameshift c.233_236del p.(Leu78Glnfs*11) variant. The fetus and the newborn had extensive brain malformations.
Sources: Literature
Intellectual disability v5.536 RNU4-2 Zornitza Stark gene: RNU4-2 was added
gene: RNU4-2 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: RNU4-2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RNU4-2 were set to 38645094
Phenotypes for gene: RNU4-2 were set to Neurodevelopmental disorder, MONDO:0700092, RNU4-2 related
Review for gene: RNU4-2 was set to GREEN
Added comment: Over 100 individuals reported with NND and heterozygous variants in a 18 bp region of RNU4-2 mapping to two structural elements in the U4/U6 snRNA duplex (the T-loop and Stem III). The vast majority of individuals (77.3%) have the same highly recurrent single base-pair insertion (n.64_65insT). Variants in this region likely explain 0.41% of individuals with NDD.
Sources: Literature
Intellectual disability v5.536 ACBD6 Arina Puzriakova Added comment: Comment on phenotypes: This gene now has a relevant phenotype listed in OMIM (MIM# 620785)
Intellectual disability v5.536 ACBD6 Arina Puzriakova Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder, MONDO:0700092 to Neurodevelopmental disorder with progressive movement abnormalities, OMIM:620785
Childhood onset dystonia, chorea or related movement disorder v3.77 ACBD6 Arina Puzriakova Added comment: Comment on phenotypes: This gene now has a relevant phenotype listed in OMIM (MIM# 620785)
Childhood onset dystonia, chorea or related movement disorder v3.77 ACBD6 Arina Puzriakova Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder, MONDO:0700092 to Neurodevelopmental disorder with progressive movement abnormalities, OMIM:620785
Childhood onset hereditary spastic paraplegia v4.43 ACBD6 Arina Puzriakova Added comment: Comment on phenotypes: This gene now has a relevant phenotype listed in OMIM (MIM# 620785)
Childhood onset hereditary spastic paraplegia v4.43 ACBD6 Arina Puzriakova Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder, MONDO:0700092 to Neurodevelopmental disorder with progressive movement abnormalities, OMIM:620785
Severe microcephaly v4.68 ACBD6 Arina Puzriakova Added comment: Comment on phenotypes: This gene now has a relevant phenotype listed in OMIM (MIM# 620785)
Severe microcephaly v4.68 ACBD6 Arina Puzriakova Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder, MONDO:0700092 to Neurodevelopmental disorder with progressive movement abnormalities, OMIM:620785
Ataxia and cerebellar anomalies - narrow panel v4.64 ACBD6 Arina Puzriakova Added comment: Comment on phenotypes: This gene now has a relevant phenotype listed in OMIM (MIM# 620785)
Ataxia and cerebellar anomalies - narrow panel v4.64 ACBD6 Arina Puzriakova Phenotypes for gene: ACBD6 were changed from Neurodevelopmental disorder, MONDO:0700092 to Neurodevelopmental disorder with progressive movement abnormalities, OMIM:620785
Paediatric disorders - additional genes v3.10 PLD1 Arina Puzriakova changed review comment from: Comment on list classification: This Green gene was signed off in Nov 2022 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.; to: Comment on list classification: This Green gene was signed off in Mar 2023 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.
Fetal anomalies v3.157 PLD1 Arina Puzriakova changed review comment from: Comment on list classification: This Green gene was signed off in Nov 2022 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.; to: Comment on list classification: This Green gene was signed off in Mar 2023 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.
Paediatric disorders - additional genes v3.10 PLD1 Arina Puzriakova Classified gene: PLD1 as Green List (high evidence)
Paediatric disorders - additional genes v3.10 PLD1 Arina Puzriakova Added comment: Comment on list classification: This Green gene was signed off in Nov 2022 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.
Paediatric disorders - additional genes v3.10 PLD1 Arina Puzriakova Gene: pld1 has been classified as Green List (High Evidence).
Fetal anomalies v3.157 PLD1 Arina Puzriakova Classified gene: PLD1 as Green List (high evidence)
Fetal anomalies v3.157 PLD1 Arina Puzriakova Added comment: Comment on list classification: This Green gene was signed off in Nov 2022 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.
Fetal anomalies v3.157 PLD1 Arina Puzriakova Gene: pld1 has been classified as Green List (High Evidence).
Fetal anomalies v3.156 PLD1 Arina Puzriakova Tag Q2_24_demote_red tag was added to gene: PLD1.
Tag Q2_24_expert_review tag was added to gene: PLD1.
Paediatric disorders - additional genes v3.9 PLD1 Arina Puzriakova Tag Q2_24_demote_red tag was added to gene: PLD1.
Tag Q2_24_expert_review tag was added to gene: PLD1.
Paediatric disorders - additional genes v3.9 PLD1 Arina Puzriakova commented on gene: PLD1: Copied review from Paediatric or syndromic cardiomyopathy (749) v3.43 panel:

Jesse Hayesmoore (Oxford Regional Genetics Laboratory)
Red List (low evidence)

"On the basis of functional data described in PMIDs: 27799408 and 33645542, PLD1 certainly seems to be a plausible functional candidate for causality of cardiac valvular defects. The main paper linking this gene with congenital heart disease / cardiomyopathy is Lahrouchi et al. (2021; PMID: 33645542; note this also includes the same 2 cases as described in Ta-Shma et al. 2017 PMID: 27799408). The paper presents 19 families with severe fetal- / neonatal-onset congenital heart (mainly valvular) defects and 2 with cardiomyopathy where affected babies were homozygous or compound heterozygous for PLD1 variants. The paper also provides some functional analysis of missense variants detected, showing that many but not all of them result significant loss of PLD1 function. Unfortunately, the paper does not include a LOD score, and there is very little cosegregation data presented for any of the variants. In addition, 4 of the 31 variants they promote as pathogenic for autosomal recessive disease are detected in multiple homozygous individuals on gnomAD, which I think provides significant evidence that they might not be pathogenic for a severe autosomal recessive condition. Most notably, 1 of the variants (i.e. I668F), which the authors promote as a pathogenic Ashkenazi Jewish founder variant (but which is also fairly frequent in non-Finnish Europeans) is detected in 7 homozygotes on gnomAD and was found to have ~80% loss of PLD1 function in their assay. This suggests that significant loss of function of this gene (i.e. down to 20%) might not be causative of a severe recessive condition (that is not to say that total or near total loss of function is not causative). Three other of the variants promoted as pathogenic in this article are also detected in homozygotes on gnomAD.

I think one of the major pieces of missing information required to make a full assessment of this gene’s linkage to disease is that is unknown how frequent biallelic (apparently loss of function) variant genotypes are in the general population or in healthy control individuals. Although homozygosity for any one variant can be determined from gnomAD, compound heterozygosity (which is likely to represent the vast majority of biallelic genotypes) cannot be assessed on gnomAD, and I can find no record in the literature of this being assessed in a normal control cohort. Without this information, we cannot know whether biallelic PLD1 genotypes are specific to babies with this severe phenotype. Without knowing this, and in the absence of any significant cosegregation data for any variant, there is no reasonable basis upon which one can conclude that this is a valid autosomal recessive gene for the phenotype. Without such validation, PVS1 cannot be applied for any apparent loss of function variant. Given this, and the general lack of cosegregation data for any one variant, I do not believe there is any PLD1 variant reported in the literature that could be classified as anything but uncertain significance (if not benign or likely benign) on the basis of current variant classification guidelines. Also, there are only two cases of biallelic variants in neonates where the primary phenotype is cardiomyopathy, and of these only one was dilated cardiomyopathy (the other was histiocytoid cardiomyopathy). Hence, the evidence linking this gene to cardiomyopathy is even weaker than it is for valvular defects. I, therefore, do not feel there is sufficient evidence to justify this gene being tested as part of the R135 paediatric cardiomyopathy gene panel.

Other papers (e.g. PMIDs: 33142350, 35380090, 36923242, 37770978) reporting a link between PLD1 genotypes and early onset cardiac disease (not cardiomyopathy) have been published. However, again, I do not think there is sufficient data in the articles to allow any of the variants detected to be confidently classified as anything but VUS according to current variant classification guidelines."
Created: 31 Jan 2024, 12:04 p.m. | Last Modified: 31 Jan 2024, 12:17 p.m
Paediatric or syndromic cardiomyopathy v3.47 PLD1 Arina Puzriakova Classified gene: PLD1 as Green List (high evidence)
Paediatric or syndromic cardiomyopathy v3.47 PLD1 Arina Puzriakova Added comment: Comment on list classification: This Green gene was signed off in Nov 2022 but now flagging for another review by the GMS specialist group in the context of the conflicting Red review by Jesse Hayesmoore (Oxford Regional Genetics Laboratory) to determine whether this gene should be downgraded.
Paediatric or syndromic cardiomyopathy v3.47 PLD1 Arina Puzriakova Gene: pld1 has been classified as Green List (High Evidence).
Fetal anomalies v3.156 PLD1 Arina Puzriakova commented on gene: PLD1: Copied review from Paediatric or syndromic cardiomyopathy (749) v3.43 panel:

Jesse Hayesmoore (Oxford Regional Genetics Laboratory)
Red List (low evidence)

"On the basis of functional data described in PMIDs: 27799408 and 33645542, PLD1 certainly seems to be a plausible functional candidate for causality of cardiac valvular defects. The main paper linking this gene with congenital heart disease / cardiomyopathy is Lahrouchi et al. (2021; PMID: 33645542; note this also includes the same 2 cases as described in Ta-Shma et al. 2017 PMID: 27799408). The paper presents 19 families with severe fetal- / neonatal-onset congenital heart (mainly valvular) defects and 2 with cardiomyopathy where affected babies were homozygous or compound heterozygous for PLD1 variants. The paper also provides some functional analysis of missense variants detected, showing that many but not all of them result significant loss of PLD1 function. Unfortunately, the paper does not include a LOD score, and there is very little cosegregation data presented for any of the variants. In addition, 4 of the 31 variants they promote as pathogenic for autosomal recessive disease are detected in multiple homozygous individuals on gnomAD, which I think provides significant evidence that they might not be pathogenic for a severe autosomal recessive condition. Most notably, 1 of the variants (i.e. I668F), which the authors promote as a pathogenic Ashkenazi Jewish founder variant (but which is also fairly frequent in non-Finnish Europeans) is detected in 7 homozygotes on gnomAD and was found to have ~80% loss of PLD1 function in their assay. This suggests that significant loss of function of this gene (i.e. down to 20%) might not be causative of a severe recessive condition (that is not to say that total or near total loss of function is not causative). Three other of the variants promoted as pathogenic in this article are also detected in homozygotes on gnomAD.

I think one of the major pieces of missing information required to make a full assessment of this gene’s linkage to disease is that is unknown how frequent biallelic (apparently loss of function) variant genotypes are in the general population or in healthy control individuals. Although homozygosity for any one variant can be determined from gnomAD, compound heterozygosity (which is likely to represent the vast majority of biallelic genotypes) cannot be assessed on gnomAD, and I can find no record in the literature of this being assessed in a normal control cohort. Without this information, we cannot know whether biallelic PLD1 genotypes are specific to babies with this severe phenotype. Without knowing this, and in the absence of any significant cosegregation data for any variant, there is no reasonable basis upon which one can conclude that this is a valid autosomal recessive gene for the phenotype. Without such validation, PVS1 cannot be applied for any apparent loss of function variant. Given this, and the general lack of cosegregation data for any one variant, I do not believe there is any PLD1 variant reported in the literature that could be classified as anything but uncertain significance (if not benign or likely benign) on the basis of current variant classification guidelines. Also, there are only two cases of biallelic variants in neonates where the primary phenotype is cardiomyopathy, and of these only one was dilated cardiomyopathy (the other was histiocytoid cardiomyopathy). Hence, the evidence linking this gene to cardiomyopathy is even weaker than it is for valvular defects. I, therefore, do not feel there is sufficient evidence to justify this gene being tested as part of the R135 paediatric cardiomyopathy gene panel.

Other papers (e.g. PMIDs: 33142350, 35380090, 36923242, 37770978) reporting a link between PLD1 genotypes and early onset cardiac disease (not cardiomyopathy) have been published. However, again, I do not think there is sufficient data in the articles to allow any of the variants detected to be confidently classified as anything but VUS according to current variant classification guidelines."
Created: 31 Jan 2024, 12:04 p.m. | Last Modified: 31 Jan 2024, 12:17 p.m
Paediatric or syndromic cardiomyopathy v3.46 PLD1 Arina Puzriakova Tag Q2_24_demote_red tag was added to gene: PLD1.
Tag Q2_24_expert_review tag was added to gene: PLD1.
Tag Q2_24_NHS_review tag was added to gene: PLD1.
Early onset or syndromic epilepsy v4.195 GLI3 Arina Puzriakova Mode of inheritance for gene: GLI3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Early onset or syndromic epilepsy v4.194 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Skeletal ciliopathies v3.22 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Childhood onset dystonia, chorea or related movement disorder v3.76 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Neurological ciliopathies v3.19 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Ophthalmological ciliopathies v3.6 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Rare multisystem ciliopathy disorders v1.171 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Joubert Syndrome and Senior-Loken Syndrome 24 gene panel to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Clefting v4.109 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Pallister-Hall syndrome, 146510 to Pallister-Hall syndrome, OMIM:146510
Rare syndromic craniosynostosis or isolated multisuture synostosis v4.180 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Greig cephalopolysyndactyly syndrome 175700; 175700 to Greig cephalopolysyndactyly syndrome, OMIM:175700
Unexplained young onset end-stage renal disease v3.41 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Pallister-Hall syndrome; Pallister-Hall syndrome 146510 to Pallister-Hall syndrome, OMIM:146510
CAKUT v1.176 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Pallister-Hall syndrome to Pallister-Hall syndrome, OMIM:146510
Unexplained kidney failure in young people v1.119 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Pallister-Hall syndrome 146510 to Pallister-Hall syndrome, OMIM:146510
Fetal anomalies v3.156 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from PALLISTER-HALL SYNDROME; GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; PREAXIAL POLYDACTYLY TYPE IV; POSTAXIAL POLYDACTYLY TYPE A to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510; Polydactyly, postaxial, types A1 and B, OMIM:174200; Polydactyly, preaxial, type IV, OMIM:174700
Skeletal dysplasia v4.57 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Greig cephalopolysyndactyly syndrome 175700; Polydactyly, postaxial, types A1 and B 174200; Polydactyly, preaxial, type IV 174700; Pallister-Hall syndrome 146510; {Hypothalamic hamartomas, somatic} 241800 to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510; Polydactyly, postaxial, types A1 and B, OMIM:174200; Polydactyly, preaxial, type IV, OMIM:174700
Limb disorders v4.19 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Greig cephalopolysyndactyly syndrome 175700; Pallister-Hall syndrome 146510; Polydactyly, postaxial, types A1 and B 174200; Polydactyly, preaxial, type IV 174700; {Hypothalamic hamartomas, somatic} 241800; Polydactyly to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510; Polydactyly, postaxial, types A1 and B, OMIM:174200; Polydactyly, preaxial, type IV, OMIM:174700
Pituitary hormone deficiency v3.12 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Greig cephalopolysyndactyly syndrome (175700); Pallister-Hall syndrome (146510) to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Intellectual disability v5.535 GLI3 Arina Puzriakova Tag Q2_24_demote_amber tag was added to gene: GLI3.
Tag Q2_24_NHS_review tag was added to gene: GLI3.
Intellectual disability v5.535 GLI3 Arina Puzriakova Phenotypes for gene: GLI3 were changed from Greig cephalopolysyndactyly syndrome, 175700Pallister-Hall syndrome, 146510Polydactyly, preaxial, type IV, 174700Polydactyly, postaxial, types A1 and B, 174200{Hypothalamic hamartomas, somatic}, 241800; GREIG CEPHALOPOLYSYNDACTYLY SYNDROME to Greig cephalopolysyndactyly syndrome, OMIM:175700; Pallister-Hall syndrome, OMIM:146510
Intellectual disability v5.534 GLI3 Arina Puzriakova Publications for gene: GLI3 were set to
Intellectual disability v5.533 GLI3 Arina Puzriakova Classified gene: GLI3 as Green List (high evidence)
Intellectual disability v5.533 GLI3 Arina Puzriakova Added comment: Comment on list classification: Reassessed in view of the Red review by Tracy Lester on this Green gene

Rarely, individuals with Greig cephalopolysyndactyly syndrome or GLI3-Related Pallister-Hall syndrome have been found to have intellectual disability (PMID: 12414818; 14708104; 14608643; 34296525). This is usually observed in the most severely affected individuals and those with large deletions encompassing GLI3. The majority of patients have normal psychomotor development or only some mild delays. All GLI3-related disorders are more likely to be recognised in context of other features such as skeletal abnormalities.

Overall, I therefore agree that this gene could be demoted to Amber at the next GMS panel update.
Intellectual disability v5.533 GLI3 Arina Puzriakova Gene: gli3 has been classified as Green List (High Evidence).
Pigmentary skin disorders v3.11 BLM Dmitrijs Rots gene: BLM was added
gene: BLM was added to Pigmentary skin disorders. Sources: Expert Review
Mode of inheritance for gene: BLM was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: BLM were set to PMID: 32972601
Phenotypes for gene: BLM were set to Bloom syndrome
Penetrance for gene: BLM were set to Complete
Review for gene: BLM was set to GREEN
Added comment: Included in the review PMID: 32972601 as differential for cafe-au-lait
Sources: Expert Review
Pigmentary skin disorders v3.11 SMARCB1 Dmitrijs Rots gene: SMARCB1 was added
gene: SMARCB1 was added to Pigmentary skin disorders. Sources: Expert Review
Mode of inheritance for gene: SMARCB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SMARCB1 were set to PMID: 32972601
Phenotypes for gene: SMARCB1 were set to Schwannomatosis-1, susceptibility to
Penetrance for gene: SMARCB1 were set to Incomplete
Review for gene: SMARCB1 was set to GREEN
Added comment: Included in the review PMID: 32972601 as differential for cafe-au-lait
Sources: Expert Review
Intellectual disability v5.532 CPA6 Arina Puzriakova Tag refuted tag was added to gene: CPA6.
Intellectual disability v5.532 CPA6 Arina Puzriakova commented on gene: CPA6
Severe microcephaly v4.67 SASS6 Zornitza Stark edited their review of gene: SASS6: Added comment: Two additional families:

PMID: 38501757
1x compound het for a fs and +3 splice variant.

Using cDNA RT-ed from mother's RNA, exons 13-15 were amplified and exon 14 was found to be skipped resulting in c.1546_1674del and p.516_558del

PMID: 36739862
1x family, compound het for 2 missense
Functional studies not performed; Changed rating: GREEN; Changed publications to: 24951542, 30639237, 38501757, 36739862
Intellectual disability v5.532 KCNB2 Zornitza Stark gene: KCNB2 was added
gene: KCNB2 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: KCNB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KCNB2 were set to 38503299
Phenotypes for gene: KCNB2 were set to neurodevelopmental disorder MONDO:0700092, KCNB2-related
Review for gene: KCNB2 was set to GREEN
Added comment: 7 individuals, all missense
5 de novo + 1x inherited from father who has hypotonia + 1x from asymptomatic father

2/5 MRI anomalies
2/5 cardiac anomalies
2/7 urogenital anomalies
7/7 with ID
2/7 epilepsy
2/7 hypotonia
Sources: Literature
Intellectual disability v5.532 GTF3C5 Zornitza Stark gene: GTF3C5 was added
gene: GTF3C5 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: GTF3C5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GTF3C5 were set to 38520561; 35503477
Phenotypes for gene: GTF3C5 were set to neurodevelopmental disorder MONDO:0700092, GTF3C5-related
Review for gene: GTF3C5 was set to GREEN
Added comment: 4 families/probands with syndromic ID. Loss of function is the expected mechanism.
PMID: 38520561 - Biallelic variants identified (3 missense & 1 stopgain) in 4 individuals from 3 families presenting with multisystem developmental syndrome including the features: growth retardation, developmental delay, intellectual disability, dental anomalies, cerebellar malformations, delayed bone age, skeletal anomalies, and facial dysmorphism. Gene-disease relationship supported by: reduced protein expression in patient cells, yeast assays, and a zebrafish model
PMID: 35503477 - 1 proband with biallelic missense variants and hypomelanosis of Ito, seizures, growth retardation, abnormal brain MRI, developmental delay, and facial dysmorphism
Sources: Literature
Intellectual disability v5.532 DOCK4 Zornitza Stark gene: DOCK4 was added
gene: DOCK4 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: DOCK4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DOCK4 were set to 38526744
Phenotypes for gene: DOCK4 were set to DOCK4-related neurodevelopmental disorder (MONDO:0060490)
Review for gene: DOCK4 was set to GREEN
Added comment: 7 unrelated individuals reported with heterozygous variants (missense or null variants) in DOCK4. The individuals either had ID or DD between mild and moderate with brain abnormalities. Two of the individuals are reportedly compound heterozygous.

Functional assay neuro-2A Dock4 knockout cells by using the Alt-R CRISPR-Cas9 system utilizing two different guide RNAs (ko1 and ko2) and one nonspecific control guide RNA (C: control). The assay depicted the loss of function mechanism in the presence of either p.Arg853Leu and p.Asp946_Lys1966delinsValSer* (described as 945VS).
Sources: Literature
Intellectual disability v5.532 PLXNB2 Zornitza Stark gene: PLXNB2 was added
gene: PLXNB2 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: PLXNB2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLXNB2 were set to 38458752
Phenotypes for gene: PLXNB2 were set to Syndromic disease MONDO:0002254, PLXNB2 -related
Review for gene: PLXNB2 was set to GREEN
Added comment: 8 individuals from 6 families with core features of amelogenesis imperfecta and sensorineural hearing loss. Intellectual disability, ocular disease, ear developmental abnormalities and lymphoedema were also present in multiple cases. WES and WGS identified biallelic pathogenic variants in PLXNB2 (missense, nonsense, splice and a multiexon deletion variants). Variants segregated with disease.

PLXNB2 is a large transmembrane semaphorin receptor protein, and semaphorin-plexin signalling controls cellular interactions that are critical during development as well as in adult life stages. Plxnb2 expression was detected in differentiating ameloblasts in mice. Human phenotype overlaps with that seen in Plxnb2 knockout mice.
Sources: Literature
Monogenic hearing loss v4.38 KIAA1024L Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: KIAA1024L.
Monogenic hearing loss v4.38 KIAA1024L Achchuthan Shanmugasundram changed review comment from: Comment on list classification: There is sufficient evidence available for the association of this gene to green rating in the next GMS review.; to: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS review.
Monogenic hearing loss v4.38 KIAA1024L Achchuthan Shanmugasundram Classified gene: KIAA1024L as Amber List (moderate evidence)
Monogenic hearing loss v4.38 KIAA1024L Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the association of this gene to green rating in the next GMS review.
Monogenic hearing loss v4.38 KIAA1024L Achchuthan Shanmugasundram Gene: kiaa1024l has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v4.37 KIAA1024L Achchuthan Shanmugasundram commented on gene: KIAA1024L: The new gene name for KIAA1024L is MINAR2 and 'new-gene-name' tag has been added to flag this.
Monogenic hearing loss v4.37 KIAA1024L Achchuthan Shanmugasundram gene: KIAA1024L was added
gene: KIAA1024L was added to Monogenic hearing loss. Sources: Literature
new-gene-name tags were added to gene: KIAA1024L.
Mode of inheritance for gene: KIAA1024L was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: KIAA1024L were set to 35727972
Phenotypes for gene: KIAA1024L were set to Deafness, autosomal recessive 120, OMIM:620238
Review for gene: KIAA1024L was set to GREEN
Added comment: PMID:35727972 reported 13 patients from four unrelated families with non-syndromic sensorineural hearing loss. Four of these patients had prelingual onset of severe to profound, progressive bilateral hearing loss. The other nine patients had congenital onset of severe to profound bilateral hearing loss, which was not progressive on one patient, while data was not available for the other.

Three different homozygous variants (c.144G > A/ p.Trp48Ter, c.412_419delCGGTTTTG/ p.Arg138Valfs*10 and c.393G > T/ p.Lys131Asn) were identified in MINAR2/ KIAA1024L gene in these patients.

There is some functional evidence available for the p.Lys131Asn variant. In addition, mice with loss of function of the Minar2 protein present with rapidly progressive sensorineural hearing loss.

This gene has also been associated with relevant phenotype in OMIM (MIM #620238).
Sources: Literature
Intellectual disability v5.532 CEP295 Zornitza Stark edited their review of gene: CEP295: Changed rating: GREEN
Intellectual disability v5.532 CEP295 Zornitza Stark gene: CEP295 was added
gene: CEP295 was added to Intellectual disability - microarray and sequencing. Sources: Expert Review
Mode of inheritance for gene: CEP295 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CEP295 were set to 38154379
Phenotypes for gene: CEP295 were set to Seckel syndrome 11, OMIM # 620767
Added comment: 4 children from 2 unrelated families with Seckel-like syndrome - severe primary microcephaly, short stature, developmental delay, intellectual disability, facial deformities, and abnormalities of fingers and toes. WES identified biallelic pathogenic variants in CEP295 gene (p(Q544∗) and p(R1520∗); p(R55Efs∗49) and p(P562L)).

Patient-derived fibroblasts and CEP295-depleted U2OS and RPE1 cells were used to clarify the underlying mechanisms. Depletion of CEP295 resulted in a decrease in the numbers of centrioles and centrosomes and triggered p53-dependent G1 cell cycle arrest. Loss of CEP295 caused extensive primary ciliary defects in both patient-derived fibroblasts and RPE1 cells. The results from complementary experiments revealed that the wild-type CEP295, but not the mutant protein, can correct the developmental defects of the centrosome/centriole and cilia in the patient-derived skin fibroblasts.
Sources: Expert Review
Ataxia and cerebellar anomalies - narrow panel v4.63 ATP2B3 Achchuthan Shanmugasundram Classified gene: ATP2B3 as Amber List (moderate evidence)
Ataxia and cerebellar anomalies - narrow panel v4.63 ATP2B3 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS update.
Ataxia and cerebellar anomalies - narrow panel v4.63 ATP2B3 Achchuthan Shanmugasundram Gene: atp2b3 has been classified as Amber List (Moderate Evidence).
Ataxia and cerebellar anomalies - narrow panel v4.62 ATP2B3 Achchuthan Shanmugasundram Publications for gene: ATP2B3 were set to
Ataxia and cerebellar anomalies - narrow panel v4.61 ATP2B3 Achchuthan Shanmugasundram Phenotypes for gene: ATP2B3 were changed from Spinocerebellar ataxia, X-linked 1 to ?Spinocerebellar ataxia, X-linked 1, OMIM:302500
Ataxia and cerebellar anomalies - narrow panel v4.60 ATP2B3 Achchuthan Shanmugasundram Mode of inheritance for gene: ATP2B3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Ataxia and cerebellar anomalies - narrow panel v4.59 ATP2B3 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: ATP2B3.
Ataxia and cerebellar anomalies - narrow panel v4.59 ATP2B3 Achchuthan Shanmugasundram changed review comment from: There are six unrelated cases reported with X-linked recessive variants in ATP2B3 gene and with a phenotype comprising ataxia. However, the onset of the disease was during childhood in three of these cases, while detailed clinical information was not available for the other three cases. There is also functional evidence available.

This gene has already been associated with ataxia in OMIM (MIM #302500), but not yet with any phenotypes in Gene2Phenotype.; to: There are six unrelated cases reported with five different X-linked recessive variants in ATP2B3 gene and with a phenotype comprising ataxia. However, the onset of the disease was during childhood in three of these cases, while detailed clinical information was not available for the other three cases. There is also functional evidence available.

This gene has already been associated with ataxia in OMIM (MIM #302500), but not yet with any phenotypes in Gene2Phenotype.
Ataxia and cerebellar anomalies - narrow panel v4.59 ATP2B3 Achchuthan Shanmugasundram reviewed gene: ATP2B3: Rating: GREEN; Mode of pathogenicity: None; Publications: 25953895, 28807751, 36207321; Phenotypes: ?Spinocerebellar ataxia, X-linked 1, OMIM:302500; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hereditary ataxia with onset in adulthood v4.34 ATP2B3 Achchuthan Shanmugasundram changed review comment from: There are six unrelated cases reported with X-linked recessive variants in ATP2B3 gene and with a phenotype comprising ataxia. However, the onset of the disease was during childhood inn three of these cases, while detailed clinical information was not available for the other three cases.; to: There are six unrelated cases reported with X-linked recessive variants in ATP2B3 gene and with a phenotype comprising ataxia. However, the onset of the disease was during childhood in three of these cases, while detailed clinical information was not available for the other three cases.
Hereditary ataxia with onset in adulthood v4.34 ATP2B3 Achchuthan Shanmugasundram Phenotypes for gene: ATP2B3 were changed from Spinocerebellar ataxia, X-linked 1; X-linked spinocerebellar ataxia, 302500 to ?Spinocerebellar ataxia, X-linked 1, OMIM:302500
Hereditary ataxia with onset in adulthood v4.33 ATP2B3 Achchuthan Shanmugasundram Publications for gene: ATP2B3 were set to
Hereditary ataxia with onset in adulthood v4.32 ATP2B3 Achchuthan Shanmugasundram Mode of inheritance for gene: ATP2B3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Hereditary ataxia with onset in adulthood v4.31 ATP2B3 Achchuthan Shanmugasundram commented on gene: ATP2B3: There are six unrelated cases reported with X-linked recessive variants in ATP2B3 gene and with a phenotype comprising ataxia. However, the onset of the disease was during childhood inn three of these cases, while detailed clinical information was not available for the other three cases.
Hereditary ataxia with onset in adulthood v4.31 ATP2B3 Achchuthan Shanmugasundram edited their review of gene: ATP2B3: Changed phenotypes to: ?Spinocerebellar ataxia, X-linked 1, OMIM:302500
Hereditary ataxia with onset in adulthood v4.31 ATP2B3 Achchuthan Shanmugasundram reviewed gene: ATP2B3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25953895, 28807751, 36207321; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Intellectual disability v5.532 SMAD3 Achchuthan Shanmugasundram changed review comment from: Two out of six cases with single nucleotide variants from DECIPHER database (https://www.deciphergenomics.org/gene/SMAD3/patient-overlap/snvs )were reported with global developmental delay. However, intellectual disability or global developmental delay were not reported as clinical presentations in patients with Loeys-Dietz syndrome 3 (MIM #613795).; to: Two out of six cases with single nucleotide variants from DECIPHER database (https://www.deciphergenomics.org/gene/SMAD3/patient-overlap/snvs) were reported with global developmental delay. However, intellectual disability or global developmental delay were not reported as clinical presentations in patients with Loeys-Dietz syndrome 3 (MIM #613795). Hence the rating should remain amber with current evidence.
Intellectual disability v5.532 SMAD3 Achchuthan Shanmugasundram reviewed gene: SMAD3: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Neurological segmental overgrowth v2.12 MAX Achchuthan Shanmugasundram Classified gene: MAX as Amber List (moderate evidence)
Neurological segmental overgrowth v2.12 MAX Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by James Poulter, there is sufficient evidence available (three unrelated cases with the same p.Arg60Gln variant and functional studies) for the promotion of this gene to green rating in the next GMS update.
Neurological segmental overgrowth v2.12 MAX Achchuthan Shanmugasundram Gene: max has been classified as Amber List (Moderate Evidence).
Neurological segmental overgrowth v2.11 MAX Achchuthan Shanmugasundram changed review comment from: PMID:38141607 reported three individuals with the same recurrent de novo germline variant in the MAX gene (p.Arg60Gln). Affected individuals have a complex disorder consisting primarily of macrocephaly, polydactyly, and delayed ophthalmic development. Other phenotypes reported include intellectual disability, perianal abscesses, pectus carinatum, hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae.

Functional analysis of the p.Arg60Gln variant shows a significant increase in CCND2 protein and a more efficient heterodimerization with c-Myc resulting in an increase in transcriptional activity of c-Myc.; to: PMID:38141607 reported three individuals with the same recurrent de novo germline variant in the MAX gene (p.Arg60Gln). Affected individuals have a complex disorder consisting primarily of macrocephaly, polydactyly, and delayed ophthalmic development. Other phenotypes reported include intellectual disability, perianal abscesses, pectus carinatum, hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae.

Functional analysis of the p.Arg60Gln variant shows a significant increase in CCND2 protein and a more efficient heterodimerization with c-Myc resulting in an increase in transcriptional activity of c-Myc.

This gene has been associated with relevant phenotypes in OMIM (MIM #620712).
Neurological segmental overgrowth v2.11 MAX Achchuthan Shanmugasundram Phenotypes for gene: MAX were changed from Macrocephaly; Polydactyly; delayed ophthalmic development; autism to Polydactyly-macrocephaly syndrome, OMIM:620712
Neurological segmental overgrowth v2.10 MAX Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: MAX.
Tag Q2_24_NHS_review tag was added to gene: MAX.
Neurological segmental overgrowth v2.10 MAX Achchuthan Shanmugasundram changed review comment from: Three individuals who each share a recurrent de novo germline variant in the MAX gene, resulting in a p.Arg60Gln substitution in the loop of the b-HLH-LZ domain.

Affected individuals have a complex disorder consisting primarily of macrocephaly, polydactyly, and delayed ophthalmic development. Other phenotypes reported include intellectual disability, perianal abscesses, pectus carinatum, hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae.

Functional analysis of the p.Arg60Gln variant shows a significant increase in CCND2 protein and a more efficient heterodimerization with c-Myc resulting in an increase in transcriptional activity of c-Myc.; to: PMID:38141607 reported three individuals with the same recurrent de novo germline variant in the MAX gene (p.Arg60Gln). Affected individuals have a complex disorder consisting primarily of macrocephaly, polydactyly, and delayed ophthalmic development. Other phenotypes reported include intellectual disability, perianal abscesses, pectus carinatum, hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae.

Functional analysis of the p.Arg60Gln variant shows a significant increase in CCND2 protein and a more efficient heterodimerization with c-Myc resulting in an increase in transcriptional activity of c-Myc.
Neurological segmental overgrowth v2.10 MAX Achchuthan Shanmugasundram Publications for gene: MAX were set to PMID:38141607
Neurological segmental overgrowth v2.9 MAX Achchuthan Shanmugasundram commented on gene: MAX: Three individuals who each share a recurrent de novo germline variant in the MAX gene, resulting in a p.Arg60Gln substitution in the loop of the b-HLH-LZ domain.

Affected individuals have a complex disorder consisting primarily of macrocephaly, polydactyly, and delayed ophthalmic development. Other phenotypes reported include intellectual disability, perianal abscesses, pectus carinatum, hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae.

Functional analysis of the p.Arg60Gln variant shows a significant increase in CCND2 protein and a more efficient heterodimerization with c-Myc resulting in an increase in transcriptional activity of c-Myc.
Neurological segmental overgrowth v2.9 MAX Achchuthan Shanmugasundram reviewed gene: MAX: Rating: GREEN; Mode of pathogenicity: None; Publications: 38141607; Phenotypes: Polydactyly-macrocephaly syndrome, OMIM:620712; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v5.532 ZFX Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has now been associated with phenotype in OMIM (MIM #301118), but not yet in Gene2Phenotype.
Intellectual disability v5.532 ZFX Achchuthan Shanmugasundram Phenotypes for gene: ZFX were changed from X-linked neurodevelopmental disorder with recurrent facial gestalt to Intellectual developmental disorder, X-linked syndromic 37, OMIM:301118
Hereditary neuropathy or pain disorder v3.94 CADM3 Achchuthan Shanmugasundram changed review comment from: Comment on list classification: As reviewed by Ian Berry, there are now five unrelated families with peripheral neuropathy and with one of the two reported missense variants in heterozygous state. Hence, this gene can be promoted to green rating in the next GMS update.; to: Comment on list classification: As reviewed by Ian Berry, there are now at least nine probands with peripheral neuropathy and with one of the two reported missense variants in heterozygous state. Hence, this gene can be promoted to green rating in the next GMS update.
Hereditary neuropathy or pain disorder v3.94 CADM3 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: CADM3.
Tag Q2_24_NHS_review tag was added to gene: CADM3.
Hereditary neuropathy or pain disorder v3.94 CADM3 Achchuthan Shanmugasundram Classified gene: CADM3 as Amber List (moderate evidence)
Hereditary neuropathy or pain disorder v3.94 CADM3 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Ian Berry, there are now five unrelated families with peripheral neuropathy and with one of the two reported missense variants in heterozygous state. Hence, this gene can be promoted to green rating in the next GMS update.
Hereditary neuropathy or pain disorder v3.94 CADM3 Achchuthan Shanmugasundram Gene: cadm3 has been classified as Amber List (Moderate Evidence).
Hereditary neuropathy or pain disorder v3.93 CADM3 Achchuthan Shanmugasundram Publications for gene: CADM3 were set to 33889941
Hereditary neuropathy or pain disorder v3.92 CADM3 Achchuthan Shanmugasundram reviewed gene: CADM3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Severe Paediatric Disorders v1.184 PRNP Tracy Lester reviewed gene: PRNP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Monogenic hearing loss v4.36 GRXCR2 Sadaf Naz reviewed gene: GRXCR2: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 33528103, PMID:24619944; Phenotypes: #615837: Deafness, autosomal recessive 101; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Paediatric or syndromic cardiomyopathy v3.46 CASZ1 Achchuthan Shanmugasundram Classified gene: CASZ1 as Amber List (moderate evidence)
Paediatric or syndromic cardiomyopathy v3.46 CASZ1 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Ludmila Volozonoka, there is sufficient evidence available (three unrelated cases and some functional studies) for the promotion of this gene to green rating in the next GMS update.
Paediatric or syndromic cardiomyopathy v3.46 CASZ1 Achchuthan Shanmugasundram Gene: casz1 has been classified as Amber List (Moderate Evidence).
Paediatric or syndromic cardiomyopathy v3.45 CASZ1 Achchuthan Shanmugasundram Phenotypes for gene: CASZ1 were changed from Pediatric Dilated Cardiomyopathy; Pediatric LVNC to dilated cardiomyopathy, MONDO:0005021; left ventricular noncompaction, MONDO:0018901
Paediatric or syndromic cardiomyopathy v3.44 CASZ1 Achchuthan Shanmugasundram changed review comment from: PMID:28099117 reported a patient with a novel heterozygous CASZ1 variant (p.K351X) and with dilated cardiomyopathy (DCM). The variant co-segregated with DCM, which was transmitted in an autosomal dominant pattern with complete penetrance. The functional characterisation of the variant with a luciferase reporter assay showed that the variant had no transcriptional activity.

PMID:31268246 reported the identification of a previously unreported de novo heterozygous frameshift variant (p.Val815Profs*14) in CASZ1 in an 11-month-old Chinese boy with DCM and left ventricular noncompaction cardiomyopathy (LVNC).

PMID:36293425 reported a girl with a new de novo frameshift variant (p.Trp1261GlyfsTer29) in CASZ1 gene. DCM was diagnosed for the first time at the age of three months and she died at the age of 1 year 10 months with a diagnosis of dilated cardiomyopathy and decompensation, systemic multiple organ failure, post-anoxic brain damage and gastrointestinal and vaginal bleeding.; to: PMID:28099117 reported a patient with a novel heterozygous CASZ1 variant (p.K351X) and with dilated cardiomyopathy (DCM). The variant co-segregated with DCM, which was transmitted in an autosomal dominant pattern with complete penetrance. The functional characterisation of the variant with a luciferase reporter assay showed that the variant had no transcriptional activity.

PMID:31268246 reported the identification of a previously unreported de novo heterozygous frameshift variant (p.Val815Profs*14) in CASZ1 in an 11-month-old Chinese boy with DCM and left ventricular noncompaction cardiomyopathy (LVNC).

PMID:36293425 reported a girl with a new de novo frameshift variant (p.Trp1261GlyfsTer29) in CASZ1 gene. DCM was diagnosed for the first time at the age of three months and she died at the age of 1 year 10 months with a diagnosis of dilated cardiomyopathy and decompensation, systemic multiple organ failure, post-anoxic brain damage and gastrointestinal and vaginal bleeding.

This gene has not yet been associated with relevant phenotypes either in OMIM or in Gene2Phenotype.
Paediatric or syndromic cardiomyopathy v3.44 CASZ1 Achchuthan Shanmugasundram edited their review of gene: CASZ1: Changed phenotypes to: dilated cardiomyopathy, MONDO:0005021, left ventricular noncompaction, MONDO:0018901
Paediatric or syndromic cardiomyopathy v3.44 CASZ1 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: CASZ1.
Paediatric or syndromic cardiomyopathy v3.44 CASZ1 Achchuthan Shanmugasundram reviewed gene: CASZ1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28099117, 31268246, 36293425; Phenotypes: dilated cardiomyopathy, MONDO:0005021; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v4.89 MT-ATP6 Achchuthan Shanmugasundram Tag Q2_24_NHS_review tag was added to gene: MT-ATP6.
Retinal disorders v4.89 SLC37A3 Achchuthan Shanmugasundram Tag Q2_24_NHS_review tag was added to gene: SLC37A3.
Retinal disorders v4.89 SLC37A3 Achchuthan Shanmugasundram Classified gene: SLC37A3 as Amber List (moderate evidence)
Retinal disorders v4.89 SLC37A3 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Siying Lin, there is sufficient evidence available for the promotion of this gene to green rating in the next GMS update.
Retinal disorders v4.89 SLC37A3 Achchuthan Shanmugasundram Gene: slc37a3 has been classified as Amber List (Moderate Evidence).
Retinal disorders v4.88 SLC37A3 Achchuthan Shanmugasundram Phenotypes for gene: SLC37A3 were changed from Retinitis pigmentosa; No OMIM entry to retinitis pigmentosa, MONDO:0019200
Retinal disorders v4.87 SLC37A3 Achchuthan Shanmugasundram Publications for gene: SLC37A3 were set to 28041643
Retinal disorders v4.86 SLC37A3 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: SLC37A3.
Retinal disorders v4.86 SLC37A3 Achchuthan Shanmugasundram reviewed gene: SLC37A3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: retinitis pigmentosa, MONDO:0019200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v4.86 MT-ATP6 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: MT-ATP6.
Retinal disorders v4.86 MT-ATP6 Achchuthan Shanmugasundram Classified gene: MT-ATP6 as Amber List (moderate evidence)
Retinal disorders v4.86 MT-ATP6 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is ample evidence available for the association of MT-ATP6 gene with retinitis pigmentosa. Hence, this gene can be promoted to green rating in the next GMS review.
Retinal disorders v4.86 MT-ATP6 Achchuthan Shanmugasundram Gene: mt-atp6 has been classified as Amber List (Moderate Evidence).
Retinal disorders v4.85 MT-ATP6 Achchuthan Shanmugasundram Phenotypes for gene: MT-ATP6 were changed from Retinitis pigmentosa to NARP syndrome, MONDO:0010794
Retinal disorders v4.84 MT-ATP6 Achchuthan Shanmugasundram Publications for gene: MT-ATP6 were set to
Retinal disorders v4.83 MT-ATP6 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: MT-ATP6.
Retinal disorders v4.83 MT-ATP6 Achchuthan Shanmugasundram reviewed gene: MT-ATP6: Rating: GREEN; Mode of pathogenicity: None; Publications: 11843698, 17568559, 19124644, 22819295, 23266623, 24118886, 27015314, 29054413, 29224958, 36809201; Phenotypes: NARP syndrome, MONDO:0010794; Mode of inheritance: MITOCHONDRIAL
Primary immunodeficiency or monogenic inflammatory bowel disease v4.201 PTCRA Achchuthan Shanmugasundram Classified gene: PTCRA as Amber List (moderate evidence)
Primary immunodeficiency or monogenic inflammatory bowel disease v4.201 PTCRA Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS update.
Primary immunodeficiency or monogenic inflammatory bowel disease v4.201 PTCRA Achchuthan Shanmugasundram Gene: ptcra has been classified as Amber List (Moderate Evidence).
Primary immunodeficiency or monogenic inflammatory bowel disease v4.200 PTCRA Achchuthan Shanmugasundram Phenotypes for gene: PTCRA were changed from Autoimmunity; elevated TCRgamma/delta T cells; lymphopenia; low TREC to Autoimmunity, HP:0002960; lymphopenia, MONDO:0003783
Primary immunodeficiency or monogenic inflammatory bowel disease v4.199 PTCRA Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: PTCRA.
Primary immunodeficiency or monogenic inflammatory bowel disease v4.199 PTCRA Achchuthan Shanmugasundram reviewed gene: PTCRA: Rating: GREEN; Mode of pathogenicity: None; Publications: 38422122; Phenotypes: Autoimmunity, HP:0002960, lymphopenia, MONDO:0003783; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v3.92 GAN Arina Puzriakova Publications for gene: GAN were set to 1106248
Hereditary neuropathy or pain disorder v3.91 GAN Arina Puzriakova Classified gene: GAN as Amber List (moderate evidence)
Hereditary neuropathy or pain disorder v3.91 GAN Arina Puzriakova Added comment: Comment on list classification: This gene should be promoted to Green at the next GMS panel update as the scope of this panel has now been expanded to include complex cases of neuropathy.
Biallelic variants in the GAN gene cause giant axonal neuropathy. This childhood onset polyneuropathy results in progressive neurodegeneration of both the peripheral and central nervous systems. More than 10 unrelated cases have been reported in the literature which is sufficient for making this gene Green (PMIDs: 18595793; 19231187; 20949505; 27852232; 36866531)
Hereditary neuropathy or pain disorder v3.91 GAN Arina Puzriakova Gene: gan has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.531 GAN Arina Puzriakova changed review comment from: Comment on list classification: Biallelic variants in the GAN gene cause giant axonal neuropathy, characterised by abnormalities in the peripheral and central nervous systems. Though extent of CNS involvement can vary, intellectual disability has been reported in at least 3 unrelated cases to date (PMID: 18595793; 19231187). Therefore, this gene should be promoted to Green at the next GMS panel update.; to: Comment on list classification: Biallelic variants in the GAN gene cause giant axonal neuropathy, characterised by abnormalities in the peripheral and central nervous systems. Though extent of CNS involvement can vary, intellectual disability has been reported in at least 3 unrelated cases (PMID: 18595793; 19231187). Therefore, this gene should be promoted to Green at the next GMS panel update.
Intellectual disability v5.531 GAN Arina Puzriakova Tag Q2_24_promote_green tag was added to gene: GAN.
Tag Q2_24_NHS_review tag was added to gene: GAN.
Intellectual disability v5.531 GAN Arina Puzriakova Publications for gene: GAN were set to
Intellectual disability v5.530 GAN Arina Puzriakova Classified gene: GAN as Amber List (moderate evidence)
Intellectual disability v5.530 GAN Arina Puzriakova Added comment: Comment on list classification: Biallelic variants in the GAN gene cause giant axonal neuropathy, characterised by abnormalities in the peripheral and central nervous systems. Though extent of CNS involvement can vary, intellectual disability has been reported in at least 3 unrelated cases to date (PMID: 18595793; 19231187). Therefore, this gene should be promoted to Green at the next GMS panel update.
Intellectual disability v5.530 GAN Arina Puzriakova Gene: gan has been classified as Amber List (Moderate Evidence).
Arthrogryposis v5.22 COASY Hannah Knight reviewed gene: COASY: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 35499143; Phenotypes: Pontocerebellar hypoplasia type 12; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v5.22 PIP5K1C Hannah Knight reviewed gene: PIP5K1C: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 38491417; Phenotypes: Lethal congenital contractural syndrome 3 611369; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v3.90 GAN Arina Puzriakova Tag Q2_24_promote_green tag was added to gene: GAN.
Tag Q2_24_NHS_review tag was added to gene: GAN.
Arthrogryposis v5.22 SLC18A3 Hannah Knight reviewed gene: SLC18A3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 34943989; Phenotypes: Myasthenic syndrome, congenital, 21, presynaptic; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v5.22 TRIP4 Hannah Knight reviewed gene: TRIP4: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 31794073; Phenotypes: Spinal muscular atrophy with congenital bone fractures 1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v5.529 GAN Arina Puzriakova Mode of inheritance for gene: GAN was changed from to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability v5.528 GAN Arina Puzriakova Phenotypes for gene: GAN were changed from to Giant axonal neuropathy-1, OMIM:256850
Hereditary neuropathy v1.477 GAN Arina Puzriakova Phenotypes for gene: GAN were changed from Giant axonal neuropathy-1 to Giant axonal neuropathy-1, OMIM:256850
Hereditary neuropathy or pain disorder v3.90 GAN Arina Puzriakova Phenotypes for gene: GAN were changed from Giant axonal neuropathy-1 to Giant axonal neuropathy-1, OMIM:256850
Intellectual disability v5.527 SEPHS1 Arina Puzriakova Classified gene: SEPHS1 as Amber List (moderate evidence)
Intellectual disability v5.527 SEPHS1 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to promote this gene to Green at the next GMS panel update.
Intellectual disability v5.527 SEPHS1 Arina Puzriakova Gene: sephs1 has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.526 SEPHS1 Arina Puzriakova Classified gene: SEPHS1 as Amber List (moderate evidence)
Intellectual disability v5.526 SEPHS1 Arina Puzriakova Gene: sephs1 has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.525 SEPHS1 Arina Puzriakova gene: SEPHS1 was added
gene: SEPHS1 was added to Intellectual disability - microarray and sequencing. Sources: Literature
Q2_24_promote_green tags were added to gene: SEPHS1.
Mode of inheritance for gene: SEPHS1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: SEPHS1 were set to 38531365
Phenotypes for gene: SEPHS1 were set to Neurodevelopmental disorder, MONDO:0700092
Review for gene: SEPHS1 was set to GREEN
Added comment: Mullegama et al. (2024) reported 9 individuals from 8 families with developmental delay, growth and feeding problems, hypotonia, and dysmorphic features, all with heterozygous missense variants in SEPHS1. Eight individuals shared different missense variants at the same p.Arg371 residue in SEPHS1 (p.Arg371Trp, p.Arg371Gln, and p.Arg371Gly); seven of these variants were confirmed as de novo (one unknown). Functional studies showed that variants at the Arg371 residue impact direct protein-protein interactions of SEPSH1 and enhance cell proliferation by modulating ROS homeostasis.
Sources: Literature
Fetal anomalies v3.155 GRM1 Arina Puzriakova Classified gene: GRM1 as Red List (low evidence)
Fetal anomalies v3.155 GRM1 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Zornitza Stark. Could not find any evidence of prenatal phenotypes in patients with GRM1 variants.
Fetal anomalies v3.155 GRM1 Arina Puzriakova Gene: grm1 has been classified as Red List (Low Evidence).
Stickler syndrome v4.4 LRP2 Arina Puzriakova Classified gene: LRP2 as Red List (low evidence)
Stickler syndrome v4.4 LRP2 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.

Only a single family reported with features overlapping those of Stickler syndrome (PMID:23992033), mainly based on their ocular phenotype, including high myopia, vitreous changes, cataract and esotropia. LRP2 variants are typically associated with Donnai-Barrow syndrome and facio-oculo-acoustico-renal syndrome which are not relevant to this panel.
Stickler syndrome v4.4 LRP2 Arina Puzriakova Gene: lrp2 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Classified gene: FCGR3B as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.

Also note review from Helen Brittain (Genomics England Clinical Team) on 100K panel Cytopenias and congenital anaemias (159) from 9 Mar 2017:

"Relevant phenotype affects neutrophils only, on a transient basis owing to presence of antibodies in mother and antigen in fetus (as a result of different genetic factors in father and mother.). Therefore not a germline condition associated with mutations in the child."
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Gene: fcgr3b has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.19 ADAMTS2 Arina Puzriakova Classified gene: ADAMTS2 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.19 ADAMTS2 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.19 ADAMTS2 Arina Puzriakova Gene: adamts2 has been classified as Red List (Low Evidence).
Dilated and arrhythmogenic cardiomyopathy v2.22 MYZAP Arina Puzriakova Tag Q2_24_promote_green tag was added to gene: MYZAP.
Dilated and arrhythmogenic cardiomyopathy v2.22 MYZAP Arina Puzriakova Deleted their comment
Dilated and arrhythmogenic cardiomyopathy v2.22 MYZAP Arina Puzriakova Publications for gene: MYZAP were set to 34899865; 20093627; 35840178
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Classified gene: MYZAP as Amber List (moderate evidence)
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Added comment: Comment on list classification: New gene added to the panel by Aleš Maver. MYZAP is not yet associated with any phenotype in OMIM or Gene2Phenoype. At least three unrelated families have been reported with biallelic LOF variants in MYZAP and a phenotype of DCM (PMIDs: 34899865; 35840178; 38436102). Studies in zebrafish and mice demonstrate the link between MYZAP and cardiomyopathy (PMIDs: 20093627; 24698889). Overall, the evidence is sufficient to promote this gene to Green at the next GMS panel update.
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Gene: myzap has been classified as Amber List (Moderate Evidence).
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Classified gene: MYZAP as Amber List (moderate evidence)
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Added comment: Comment on list classification: New gene added to the panel by Aleš Maver. MYZAP is not yet associated with any phenotype in OMIM or Gene2Phenoype. At least three unrelated families have been reported with biallelic LOF variants in MYZAP and a phenotype of DCM (PMIDs: 34899865; 35840178; 38436102). Studies in zebrafish and mice demonstrate the link between MYZAP and cardiomyopathy (PMIDs: 20093627; 24698889). Overall, the evidence is sufficient to promote this gene to Green at the next GMS panel update.
Dilated and arrhythmogenic cardiomyopathy v2.21 MYZAP Arina Puzriakova Gene: myzap has been classified as Amber List (Moderate Evidence).
Hypogonadotropic hypogonadism (GMS) v3.18 NDNF Arina Puzriakova Classified gene: NDNF as Green List (high evidence)
Hypogonadotropic hypogonadism (GMS) v3.18 NDNF Arina Puzriakova Added comment: Comment on list classification: Gene was re-reviewed in light of an Amber review by Zornitza Stark (Australian Genomics) on a Green gene. At least five unrelated cases have been reported, as well as mouse and zebrafish studies showing Ndnf deficiency leads to anomalies in GnRH neuron migration. Pedigree analysis does indicate variable expressivity and incomplete penetrance, although this is relatively common in dominant forms of HH. Furthermore, inclusion of NDNF on this panel has already been reviewed and approved by the NHS specialist group and therefore the Green rating is being maintained.
Hypogonadotropic hypogonadism (GMS) v3.18 NDNF Arina Puzriakova Gene: ndnf has been classified as Green List (High Evidence).
Hypogonadotropic hypogonadism (GMS) v3.17 NDNF Arina Puzriakova Phenotypes for gene: NDNF were changed from Congenital hypogonadotropic hypogonadism (CHH); Hypogonadotropic hypogonadism 25 with anosmia, 618841 to Hypogonadotropic hypogonadism 25 with anosmia, OMIM:618841
Hypogonadotropic hypogonadism (GMS) v3.16 NDNF Arina Puzriakova Publications for gene: NDNF were set to 31883645
Hypogonadotropic hypogonadism (GMS) v3.15 NDNF Arina Puzriakova commented on gene: NDNF: PMID: 36245975 (2022) - another male patient with idiopathic hypogonadotropin hypogonadism identified harbouring a paternally inherited NDNF variant (c.1439T>A, p.Ile480Asn)
Hereditary spastic paraplegia v1.311 RTN2 Achchuthan Shanmugasundram Added comment: Comment on mode of inheritance: As there are sufficient number of cases with biallelic variants and lower limb spasticity, the MOI has been updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal'.
Hereditary spastic paraplegia v1.311 RTN2 Achchuthan Shanmugasundram Mode of inheritance for gene: RTN2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary spastic paraplegia v1.310 RTN2 Achchuthan Shanmugasundram Phenotypes for gene: RTN2 were changed from Spastic paraplegia 12, autosomal dominant to Spastic paraplegia 12, autosomal dominant, OMIM:604805; distal hereditary motor neuropathy, MONDO:0018894; Lower limb spasticity, HP:0002061
Hereditary spastic paraplegia v1.309 RTN2 Achchuthan Shanmugasundram Publications for gene: RTN2 were set to Montenegro et al. (2012)
Hereditary spastic paraplegia v1.308 RTN2 Achchuthan Shanmugasundram reviewed gene: RTN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 38527963; Phenotypes: distal hereditary motor neuropathy, MONDO:0018894, Lower limb spasticity, HP:0002061; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Childhood onset hereditary spastic paraplegia v4.42 RTN2 Achchuthan Shanmugasundram Added comment: Comment on mode of inheritance: As there are sufficient number of cases with biallelic variants and lower limb spasticity, the MOI should be updated to 'BOTH monoallelic and biallelic, autosomal or pseudoautosomal' in the next GMS update.
Childhood onset hereditary spastic paraplegia v4.42 RTN2 Achchuthan Shanmugasundram Mode of inheritance for gene: RTN2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Childhood onset hereditary spastic paraplegia v4.41 RTN2 Achchuthan Shanmugasundram Phenotypes for gene: RTN2 were changed from Spastic paraplegia 12, autosomal dominant, 604805 to Spastic paraplegia 12, autosomal dominant, OMIM:604805; distal hereditary motor neuropathy, MONDO:0018894; Lower limb spasticity, HP:0002061
Childhood onset hereditary spastic paraplegia v4.40 RTN2 Achchuthan Shanmugasundram Publications for gene: RTN2 were set to 22232211; 24123792; 28362824
Childhood onset hereditary spastic paraplegia v4.39 RTN2 Achchuthan Shanmugasundram Tag Q2_24_MOI tag was added to gene: RTN2.
Tag Q2_24_NHS_review tag was added to gene: RTN2.
Hereditary neuropathy or pain disorder v3.89 RTN2 Achchuthan Shanmugasundram changed review comment from: PMID:38527963 reported the identification of seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven unrelated families with distal hereditary motor neuropathy.

All affected individuals exhibited weakness in the distal upper and lower limbs, lower limb spasticity, hyperreflexia, with an onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography.

Characterisation of C. elegans RTN2 homolog loss-of-function variants demonstrated morphological and behavioural differences compared to the parental strain and treatment with an endoplasmic/sarcoplasmic reticulum Ca(2+) re-uptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences.

Biallelic variants in RTN2 gene have not yet been associated with any phenotypes in OMIM or Gene2Phenotype, while monoallelic variants have been associated with spastic paraplegia (MIM #604805) in OMIM.
Sources: Literature; to: PMID:38527963 reported the identification of seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven unrelated families with distal hereditary motor neuropathy.

All affected individuals exhibited weakness in the distal upper and lower limbs, lower limb spasticity, hyperreflexia, with an onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography.

Characterisation of C. elegans RTN2 homolog loss-of-function variants demonstrated morphological and behavioural differences compared to the parental strain, and treatment with an endoplasmic/sarcoplasmic reticulum Ca(2+) re-uptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences.

Biallelic variants in RTN2 gene have not yet been associated with any phenotypes in OMIM or Gene2Phenotype, while monoallelic variants have been associated with spastic paraplegia (MIM #604805) in OMIM.
Sources: Literature
Childhood onset hereditary spastic paraplegia v4.39 RTN2 Achchuthan Shanmugasundram reviewed gene: RTN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 38527963; Phenotypes: distal hereditary motor neuropathy, MONDO:0018894, Lower limb spasticity, HP:0002061; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v3.89 RTN2 Achchuthan Shanmugasundram changed review comment from: PMID:38527963 reported the identification of seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven unrelated families with distal hereditary motor neuropathy.

All affected individuals (seven males and seven females, aged 9-50 years) exhibited weakness in the distal upper and lower limbs, lower limb spasticity, hyperreflexia, with an onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography.

Characterisation of C. elegans RTN2 homolog loss-of-function variants demonstrated morphological and behavioural differences compared to the parental strain and treatment with an endoplasmic/sarcoplasmic reticulum Ca(2+) re-uptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences.

Biallelic variants in RTN2 gene have not yet been associated with any phenotypes in OMIM or Gene2Phenotype, while monoallelic variants have been associated with spastic paraplegia (MIM #604805) in OMIM.
Sources: Literature; to: PMID:38527963 reported the identification of seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven unrelated families with distal hereditary motor neuropathy.

All affected individuals exhibited weakness in the distal upper and lower limbs, lower limb spasticity, hyperreflexia, with an onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography.

Characterisation of C. elegans RTN2 homolog loss-of-function variants demonstrated morphological and behavioural differences compared to the parental strain and treatment with an endoplasmic/sarcoplasmic reticulum Ca(2+) re-uptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences.

Biallelic variants in RTN2 gene have not yet been associated with any phenotypes in OMIM or Gene2Phenotype, while monoallelic variants have been associated with spastic paraplegia (MIM #604805) in OMIM.
Sources: Literature
Rare genetic inflammatory skin disorders v3.18 COL5A2 Arina Puzriakova Classified gene: COL5A2 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.18 COL5A2 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.18 COL5A2 Arina Puzriakova Gene: col5a2 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.17 COL5A1 Arina Puzriakova Classified gene: COL5A1 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.17 COL5A1 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.17 COL5A1 Arina Puzriakova Gene: col5a1 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.16 COL4A5 Arina Puzriakova Classified gene: COL4A5 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.16 COL4A5 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.16 COL4A5 Arina Puzriakova Gene: col4a5 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.15 COL4A4 Arina Puzriakova Classified gene: COL4A4 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.15 COL4A4 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.15 COL4A4 Arina Puzriakova Gene: col4a4 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.14 COL4A3 Arina Puzriakova Classified gene: COL4A3 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.14 COL4A3 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.14 COL4A3 Arina Puzriakova Gene: col4a3 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.13 COL3A1 Arina Puzriakova Classified gene: COL3A1 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.13 COL3A1 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.13 COL3A1 Arina Puzriakova Gene: col3a1 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.12 COL1A2 Arina Puzriakova Classified gene: COL1A2 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.12 COL1A2 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.12 COL1A2 Arina Puzriakova Gene: col1a2 has been classified as Red List (Low Evidence).
Rare genetic inflammatory skin disorders v3.11 COL1A1 Arina Puzriakova Classified gene: COL1A1 as Red List (low evidence)
Rare genetic inflammatory skin disorders v3.11 COL1A1 Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.
Rare genetic inflammatory skin disorders v3.11 COL1A1 Arina Puzriakova Gene: col1a1 has been classified as Red List (Low Evidence).
Autoinflammatory disorders v1.17 IL17RA Arina Puzriakova Tag watchlist tag was added to gene: IL17RA.
Autoinflammatory disorders v1.17 IL17RA Arina Puzriakova Classified gene: IL17RA as Amber List (moderate evidence)
Autoinflammatory disorders v1.17 IL17RA Arina Puzriakova Added comment: Comment on list classification: New gene added to this panel by Lauma Freimane (Children's Clinical University Hospital). Biallelic variants have been found patients with immunodeficiency, presenting as chronic mucocutaneous candidiasis (PMID: 21350122).

Interleukin-17A (IL-17A) is a pro-inflammatory cytokine implicated in diverse autoimmune and inflammatory disorders such as psoriasis and Kawasaki disease so it is plausible that the interleukin-17A receptor (IL-17RA) could contribute to the same pathway.

Literature review did reveal multiple mouse models where IL-17RA was shown to promote the inflammatory response (PMID: 38060620; 30364284; 35844540; 38451335); however, there is no evidence of human cases where a variant in the IL17RA gene caused an autoinflammatory disorder. Therefore rating as Amber with a watchlist tag, awaiting further evidence.
Autoinflammatory disorders v1.17 IL17RA Arina Puzriakova Gene: il17ra has been classified as Amber List (Moderate Evidence).
Primary immunodeficiency or monogenic inflammatory bowel disease v4.199 IL17RA Arina Puzriakova Added comment: Comment on phenotypes: Previous phenotypes: Candidiasis, familial, 5;Chronic mucocutaneous candidiasis (CMC);Immunodeficiency 51, 613953;Defects in Intrinsic and Innate Immunity;CMC, folliculitis;Defects in Intrinsic and Innate Immunity
Primary immunodeficiency or monogenic inflammatory bowel disease v4.199 IL17RA Arina Puzriakova Phenotypes for gene: IL17RA were changed from Candidiasis, familial, 5; Chronic mucocutaneous candidiasis (CMC); Immunodeficiency 51, 613953; Defects in Intrinsic and Innate Immunity; CMC, folliculitis; Defects in Intrinsic and Innate Immunity to Immunodeficiency 51, OMIM:613953
Autoinflammatory disorders v1.16 IL17RA Arina Puzriakova Phenotypes for gene: IL17RA were changed from Immunodeficiency-51 to Immunodeficiency 51, OMIM:613953
Likely inborn error of metabolism v4.137 ADA Arina Puzriakova Added comment: Comment on phenotypes: Previous phenotypes: Combined B and T cell defect;Adenosine deaminase deficiency (Disorders of purine metabolism);SCID;Infantile enterocolitis & monogenic inflammatory bowel disease
Likely inborn error of metabolism v4.137 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700 to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Likely inborn error of metabolism v4.136 ADA Arina Puzriakova Added comment: Comment on phenotypes: Previous phenotypes: Combined B and T cell defect;Adenosine deaminase deficiency (Disorders of purine metabolism);SCID;Infantile enterocolitis & monogenic inflammatory bowel disease
Likely inborn error of metabolism v4.136 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Combined B and T cell defect; Adenosine deaminase deficiency (Disorders of purine metabolism); SCID; Infantile enterocolitis & monogenic inflammatory bowel disease to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Primary immunodeficiency or monogenic inflammatory bowel disease v4.198 ADA Arina Puzriakova Added comment: Comment on phenotypes: Previous phenotypes: Severe combined immunodeficiency due to ADA deficiency (some mosiacism noted);Severe combined immunodeficiency due to ADA deficiency, 102700;T-B- SCID;T-B+ SCID;Adenosine deaminase (ADA) deficiency;Atypical Severe Combined Immunodeficiency (Atypical SCID);Omenn syndrome;Severe combined immunodeficiency (SCID);Low NK, bone defects, may have pulmonary alveolar proteinosis, cognitive defects;Immunodeficiencies affecting cellular and humoral immunity
Primary immunodeficiency or monogenic inflammatory bowel disease v4.198 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Severe combined immunodeficiency due to ADA deficiency (some mosiacism noted); Severe combined immunodeficiency due to ADA deficiency, 102700; T-B- SCID; T-B+ SCID; Adenosine deaminase (ADA) deficiency; Atypical Severe Combined Immunodeficiency (Atypical SCID); Omenn syndrome; Severe combined immunodeficiency (SCID); Low NK, bone defects, may have pulmonary alveolar proteinosis, cognitive defects; Immunodeficiencies affecting cellular and humoral immunity to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Fetal anomalies v3.154 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Combined B and T cell defect; Adenosine deaminase deficiency (Disorders of purine metabolism); SCID; Infantile enterocolitis & monogenic inflammatory bowel disease to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Fetal anomalies v3.153 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from ADENOSINE DEAMINASE DEFICIENCY to Combined B and T cell defect; Adenosine deaminase deficiency (Disorders of purine metabolism); SCID; Infantile enterocolitis & monogenic inflammatory bowel disease
Undiagnosed metabolic disorders v1.617 ADA Arina Puzriakova Added comment: Comment on phenotypes: Previous phenotypes: Adenosine deaminase deficiency (Disorders of purine metabolism);Combined B and T cell defect;Infantile enterocolitis & monogenic inflammatory bowel disease;SCID
Undiagnosed metabolic disorders v1.617 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Adenosine deaminase deficiency (Disorders of purine metabolism); Combined B and T cell defect; Infantile enterocolitis & monogenic inflammatory bowel disease; SCID to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Intellectual disability v5.524 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Severe combined immunodeficiency due to ADA deficiency, 102700; Adenosine deaminase deficiency, partial, 102700 to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Severe combined immunodeficiency with adenosine deaminase deficiency v1.3 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700 to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700
Severe combined immunodeficiency with adenosine deaminase deficiency v1.2 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Autoinflammatory disorders v1.15 ADA Arina Puzriakova Phenotypes for gene: ADA were changed from T(-), B(-), NK(-) severe combin immunodeficiency to Severe combined immunodeficiency due to ADA deficiency, OMIM:102700; Adenosine deaminase deficiency, partial, OMIM:102700
Bleeding and platelet disorders v3.9 GP6 Arina Puzriakova Phenotypes for gene: GP6 were changed from 614201 Bleeding disorder, platelet-type, 11 to Bleeding disorder, platelet-type, 11, OMIM:614201
Inherited bleeding disorders v1.177 GP6 Arina Puzriakova Phenotypes for gene: GP6 were changed from Bleeding diathesis due to glycoprotein VI deficiency to Bleeding disorder, platelet-type, 11, OMIM:614201
Autoinflammatory disorders v1.14 GP6 Arina Puzriakova Phenotypes for gene: GP6 were changed from Platlet-type bleeding disorder-11 to Bleeding disorder, platelet-type, 11, OMIM:614201
Autoinflammatory disorders v1.13 GP6 Arina Puzriakova Classified gene: GP6 as Red List (low evidence)
Autoinflammatory disorders v1.13 GP6 Arina Puzriakova Added comment: Comment on list classification: New gene added to this panel by Lauma Freimane (Children's Clinical University Hospital). Biallelic variants are associated with bleeding disorder caused by defective platelet activation and aggregation in response to collagen. Could not find evidence of an autoinflammatory component observed in patients and therefore rating as Red on this panel
Autoinflammatory disorders v1.13 GP6 Arina Puzriakova Gene: gp6 has been classified as Red List (Low Evidence).
Autoinflammatory disorders v1.12 ADA Arina Puzriakova Classified gene: ADA as Red List (low evidence)
Autoinflammatory disorders v1.12 ADA Arina Puzriakova Added comment: Comment on list classification: New gene added to this panel by Lauma Freimane (Children's Clinical University Hospital). Biallelic variants are associated with partial ADA deficiency or severe combined immunodeficiency (SCID) due to ADA deficiency with multiple unrelated cases reported.

Despite ADA null mice displaying severe pulmonary inflammation, could not find evidence of an autoinflammatory component observed in patients and therefore rating as Red on this panel
Autoinflammatory disorders v1.12 ADA Arina Puzriakova Gene: ada has been classified as Red List (Low Evidence).
Hereditary neuropathy or pain disorder v3.89 RTN2 Achchuthan Shanmugasundram Classified gene: RTN2 as Amber List (moderate evidence)
Hereditary neuropathy or pain disorder v3.89 RTN2 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the association of RTN2 biallelic variants with distal hereditary motor neuropathy. Hence, this gene should be promoted to green rating in the next GMS update.
Hereditary neuropathy or pain disorder v3.89 RTN2 Achchuthan Shanmugasundram Gene: rtn2 has been classified as Amber List (Moderate Evidence).
Hereditary neuropathy or pain disorder v3.88 RTN2 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: RTN2.
Hereditary neuropathy or pain disorder v3.88 RTN2 Achchuthan Shanmugasundram gene: RTN2 was added
gene: RTN2 was added to Hereditary neuropathy or pain disorder. Sources: Literature
Mode of inheritance for gene: RTN2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RTN2 were set to 38527963
Phenotypes for gene: RTN2 were set to distal hereditary motor neuropathy, MONDO:0018894
Review for gene: RTN2 was set to GREEN
Added comment: PMID:38527963 reported the identification of seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven unrelated families with distal hereditary motor neuropathy.

All affected individuals (seven males and seven females, aged 9-50 years) exhibited weakness in the distal upper and lower limbs, lower limb spasticity, hyperreflexia, with an onset in the first decade of life. Nerve conduction studies revealed axonal motor neuropathy with neurogenic changes in the electromyography.

Characterisation of C. elegans RTN2 homolog loss-of-function variants demonstrated morphological and behavioural differences compared to the parental strain and treatment with an endoplasmic/sarcoplasmic reticulum Ca(2+) re-uptake inhibitor (2,5-di-tert-butylhydroquinone) rescued key phenotypic differences.

Biallelic variants in RTN2 gene have not yet been associated with any phenotypes in OMIM or Gene2Phenotype, while monoallelic variants have been associated with spastic paraplegia (MIM #604805) in OMIM.
Sources: Literature
Fetal anomalies v3.152 NRXN2 Sarah Leigh Classified gene: NRXN2 as Red List (low evidence)
Fetal anomalies v3.152 NRXN2 Sarah Leigh Added comment: Comment on list classification: There insufficient evidence between NRXN2 variants and autism for this gene to be rated amber.
Fetal anomalies v3.152 NRXN2 Sarah Leigh Gene: nrxn2 has been classified as Red List (Low Evidence).
Iron metabolism disorders - NOT common HFE mutations v2.6 CYBRD1 Sarah Leigh Publications for gene: CYBRD1 were set to 15338274; 27884173
Iron metabolism disorders - NOT common HFE mutations v2.5 CYBRD1 Sarah Leigh edited their review of gene: CYBRD1: Added comment: It would appear that there are no CYBRD1 rare SNVs associated with iron metabolism.  However, PMID: 37632052 concludes that the coexistence of minor alleles of HDAC3 rs976552 and CYBRD1 rs884409 is linked with higher prevalence of hepatocellular carcinoma.

Furthermore, HFE p.C282Y variant together with the CYBRD1 polymorphism rs884409 reduces CYBRD1 promoter activity by 30% (PMID: 19673882).; Changed rating: AMBER
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova changed review comment from: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent heterozygous LIM2 p.R130C variant (PMIDs: 32202185; 33078099; 33708862; 33923544; 35736209). These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.; to: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with cataracts due to a recurrent heterozygous LIM2 p.R130C variant (PMIDs: 32202185; 33078099; 33708862; 33923544; 35736209). These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova changed review comment from: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent LIM2 p.R130C variant (PMIDs: 32202185; 33078099; 33708862; 33923544; 35736209). These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.; to: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent heterozygous LIM2 p.R130C variant (PMIDs: 32202185; 33078099; 33708862; 33923544; 35736209). These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova Tag recurrent-variant tag was added to gene: LIM2.
Tag Q2_24_MOI tag was added to gene: LIM2.
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova changed review comment from: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent LIM2 p.R130C variant. These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.; to: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent LIM2 p.R130C variant (PMIDs: 32202185; 33078099; 33708862; 33923544; 35736209). These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova Added comment: Comment on mode of inheritance: The MOI should be updated from 'biallelic' to 'both mono- and biallelic' at the next GMS panel update. At least 9 unrelated multigenerational families have been identified with congenital cataracts due to a recurrent LIM2 p.R130C variant. These families come from different ancestries (British, Chinese, Spanish, Japanese) and haplotype analysis in families from shared ancestries has suggested the variant likely arose due to independent founder events in each family. The evidence therefore supports this MOI being included in future analyses.
Bilateral congenital or childhood onset cataracts v4.12 LIM2 Arina Puzriakova Mode of inheritance for gene: LIM2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Hereditary neuropathy or pain disorder v3.87 CADM3 Ian Berry reviewed gene: CADM3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 38074074, 33889941; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bilateral congenital or childhood onset cataracts v4.11 LIM2 Arina Puzriakova Publications for gene: LIM2 were set to Ponnam et al (2008) Mol Vis 14:1204-1208; Pras et al (2002) Am J Hum genet 70:1363-7
Bilateral congenital or childhood onset cataracts v4.10 LIM2 Arina Puzriakova Phenotypes for gene: LIM2 were changed from Cortical Pulverulent Cataract; Cataract 19, 615277 to Cataract 19, multiple types, OMIM:615277
Structural eye disease v3.77 LIM2 Arina Puzriakova Phenotypes for gene: LIM2 were changed from Cataract 19, 615277 to Cataract 19, multiple types, OMIM:615277
Intellectual disability v5.523 FRYL Arina Puzriakova Classified gene: FRYL as Amber List (moderate evidence)
Intellectual disability v5.523 FRYL Arina Puzriakova Added comment: Comment on list classification: Rating Amber as overall the evidence is borderline. Only one recent study (PMID:38479391) has reported an disease association for FRYL, with variable phenotypes and results from functional studies, as well as variants in other genes in several cases. Additional studies are required to conclusively corroborate causality (added watchlist tag).
Intellectual disability v5.523 FRYL Arina Puzriakova Gene: fryl has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.522 FRYL Arina Puzriakova gene: FRYL was added
gene: FRYL was added to Intellectual disability - microarray and sequencing. Sources: Literature
watchlist tags were added to gene: FRYL.
Mode of inheritance for gene: FRYL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: FRYL were set to 38479391
Phenotypes for gene: FRYL were set to Neurodevelopmental disorder, MONDO:0700092
Review for gene: FRYL was set to AMBER
Added comment: New association linking this gene to disease which is not yet listed in OMIM or Gene2Phenotype. There are no sequence variants in Decipher and ClinVar shows only a single pathogenic frameshift variant (c.1224del, p.Lys409fs) for FRYL-associated neurodevelopmental disorder, amongst multiple SNVs which are mostly missense VUS or B/LB.

Pan et al., 2024 (PMID: 38479391) reported 14 individuals with heterozygous variant in FRYL who presented with DD/ID, dysmorphic features, and other congenital anomalies in multiple systems. Except for DD/ID which was the only universal feature, observed phenotypes were variable and nonspecific.

Variants were confirmed de novo in all except one individual (duo testing excluded paternal inheritance although it was present at low frequency in gnomAD). Variant types include missense (5), fs/stop-gain (8) and canonical splice (1). Modelling 4/5 patient missense variants using flies showed that only one serves as a severe LoF variant, two others behave as partial LoF variants, and one variant had no functional impact (only variant not confirmed as de novo indicating this is a VUS). Four individuals also had P/LP variants in other genes (SF3B4, DHCR7, SLC6A19, SDHA) which could at least partially explain their phenotypes, and a further four harboured additional VUSs.
Sources: Literature
RASopathies v1.81 RRAS Sarah Leigh Classified gene: RRAS as Green List (high evidence)
RASopathies v1.81 RRAS Sarah Leigh Gene: rras has been classified as Green List (High Evidence).
RASopathies v1.80 RRAS Sarah Leigh Tag Q2_24_promote_green was removed from gene: RRAS.
RASopathies v1.80 RRAS Sarah Leigh Tag Q2_24_promote_green tag was added to gene: RRAS.
Fetal anomalies v3.151 RRAS Sarah Leigh Tag Q2_24_promote_green tag was added to gene: RRAS.
Cytopenia - NOT Fanconi anaemia v3.31 RRAS Sarah Leigh Tag Q2_24_promote_green tag was added to gene: RRAS.
RASopathies v1.80 RRAS Sarah Leigh Publications for gene: RRAS were set to 24705357
RASopathies v1.79 RRAS Sarah Leigh edited their review of gene: RRAS: Added comment: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.; Changed rating: GREEN; Changed publications to: 24705357, 32815881, 34935735
Fetal anomalies v3.151 RRAS Sarah Leigh edited their review of gene: RRAS: Added comment: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.; Changed rating: GREEN; Changed publications to: 24705357, 32815881, 34935735
Cytopenia - NOT Fanconi anaemia v3.31 RRAS Sarah Leigh Publications for gene: RRAS were set to 34935735
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh commented on gene: RRAS: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.
RASopathies v1.79 RRAS Sarah Leigh Added comment: Comment on phenotypes: Phenotype from Gen2Phen
RASopathies v1.79 RRAS Sarah Leigh Phenotypes for gene: RRAS were changed from Noonan syndrome to RRAS-related atypical Noonan syndrome
Fetal anomalies v3.151 RRAS Sarah Leigh Added comment: Comment on phenotypes: Phenotype from Gen2Phen
Fetal anomalies v3.151 RRAS Sarah Leigh Phenotypes for gene: RRAS were changed from ATYPICAL NOONAN SYNDROME to RRAS-related atypical Noonan syndrome
Fetal anomalies v3.150 RRAS Sarah Leigh Publications for gene: RRAS were set to
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh edited their review of gene: RRAS: Added comment: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.; Changed rating: GREEN; Changed publications to: 24705357, 32815881, 34935735; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh Added comment: Comment on phenotypes: RRAS-related atypical Noonan syndrome phenotype from Gen2Phen
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh Phenotypes for gene: RRAS were changed from Pediatric Myelodysplastic Syndrome to RRAS-related atypical Noonan syndrome
Cytopenia - NOT Fanconi anaemia v3.29 RRAS Sarah Leigh Publications for gene: RRAS were set to PMID: 34935735
Cytopenia - NOT Fanconi anaemia v3.28 RRAS Sarah Leigh Classified gene: RRAS as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.28 RRAS Sarah Leigh Gene: rras has been classified as Amber List (Moderate Evidence).
Hereditary ataxia with onset in adulthood v4.31 NAA60 Sarah Leigh commented on gene: NAA60: NAA60 should be green on the Hereditary ataxia with onset in adulthood as four of the families described in table 1 (PMID: 38480682), also displayed either cerebellar syndrome (which often includes ataxia) or cerebellar ataxia (personal communication from Helen Brittain (Genomics England Clinical Fellow).
Adult onset neurodegenerative disorder v4.47 NAA60 Sarah Leigh changed review comment from: To date, NAA60 variants are not associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38480682 reports six NAA60 variants in six unrelated cases with an autosomal recessive primary familial brain calcification (PFBC). Table 2 in PMID: 38480682 outlines the extent of the calcification seen in the patient's CT scans. Functional studies show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro, and loss of function by the NAA60 variants results in a reduced level of surface SLC20A2, thereby, reducing the extracellular phosphate uptake. The authors conclude, that this study provides a possible biochemical explanation of the involvement of NAA60 variants in PFBC development (PMID: 38480682).
Sources: Literature; to: To date, NAA60 variants are not associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38480682 reports six NAA60 variants in six unrelated cases with an autosomal recessive primary familial brain calcification (PFBC); signs of Parkinsonian presentation was evident in three families reported. Table 2 in PMID: 38480682 outlines the extent of the calcification seen in the patient's CT scans. Functional studies show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro, and loss of function by the NAA60 variants results in a reduced level of surface SLC20A2, thereby, reducing the extracellular phosphate uptake. The authors conclude, that this study provides a possible biochemical explanation of the involvement of NAA60 variants in PFBC development (PMID: 38480682).
Sources: Literature
Hereditary ataxia with onset in adulthood v4.31 NAA60 Sarah Leigh Tag Q2_24_MOI tag was added to gene: NAA60.
Adult onset neurodegenerative disorder v4.47 NAA60 Sarah Leigh Tag Q2_24_MOI tag was added to gene: NAA60.
White matter disorders and cerebral calcification - narrow panel v3.35 NAA60 Sarah Leigh Tag Q2_24_MOI tag was added to gene: NAA60.
Hereditary ataxia with onset in adulthood v4.31 NAA60 Sarah Leigh Entity copied from White matter disorders and cerebral calcification - narrow panel v3.35
Hereditary ataxia with onset in adulthood v4.31 NAA60 Sarah Leigh gene: NAA60 was added
gene: NAA60 was added to Hereditary ataxia with onset in adulthood. Sources: Literature,Expert Review Amber
Q2_24_promote_green, Q2_24_NHS_review tags were added to gene: NAA60.
Mode of inheritance for gene: NAA60 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NAA60 were set to 38480682
Phenotypes for gene: NAA60 were set to NAA60 associated autosomal recessive primary familial brain calcifications
Adult onset neurodegenerative disorder v4.47 NAA60 Sarah Leigh Entity copied from White matter disorders and cerebral calcification - narrow panel v3.35
Adult onset neurodegenerative disorder v4.47 NAA60 Sarah Leigh gene: NAA60 was added
gene: NAA60 was added to Adult onset neurodegenerative disorder. Sources: Literature,Expert Review Amber
Q2_24_promote_green, Q2_24_NHS_review tags were added to gene: NAA60.
Mode of inheritance for gene: NAA60 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NAA60 were set to 38480682
Phenotypes for gene: NAA60 were set to NAA60 associated autosomal recessive primary familial brain calcifications
White matter disorders and cerebral calcification - narrow panel v3.35 NAA60 Sarah Leigh changed review comment from: To date, NAA60 variants are not associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38480682 reports six NAA60 variants in six unrelated cases with an autosomal recessive primary familial brain calcification (PFBC). Table 2 in PMID: 38480682 outlines the extent of the calcification seen in the patient's CT scans. Functional studies show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro, and loss of function by the NAA60 variants results in a reduced level of surface SLC20A2, thereby, reducing the extracellular phosphate uptake. The authors conclude, that this study provides a possible biochemical explanation of the involvement of NAA60 variants in PFBC development (PMID: 38480682).
Sources: Literature; to: To date, NAA60 variants are not associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38480682 reports six NAA60 variants in six unrelated cases with an autosomal recessive primary familial brain calcification (PFBC). Table 2 in PMID: 38480682 outlines the extent of the calcification seen in the patient's CT scans. Functional studies show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro, and loss of function by the NAA60 variants results in a reduced level of surface SLC20A2, thereby, reducing the extracellular phosphate uptake. The authors conclude, that this study provides a possible biochemical explanation of the involvement of NAA60 variants in PFBC development (PMID: 38480682).
Sources: Literature
White matter disorders and cerebral calcification - narrow panel v3.35 NAA60 Sarah Leigh Mode of inheritance for gene: NAA60 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BIALLELIC, autosomal or pseudoautosomal
Optic neuropathy v4.30 BTD Achchuthan Shanmugasundram Phenotypes for gene: BTD were changed from Biotinidase deficiency, OMIM:253260 to Biotinidase deficiency, OMIM:253260; optic atrophy, MONDO:0003608
Optic neuropathy v4.29 BTD Achchuthan Shanmugasundram edited their review of gene: BTD: Changed phenotypes to: Biotinidase deficiency, OMIM:253260, optic atrophy, MONDO:0003608
Optic neuropathy v4.29 BTD Achchuthan Shanmugasundram Classified gene: BTD as Amber List (moderate evidence)
Optic neuropathy v4.29 BTD Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS review.
Optic neuropathy v4.29 BTD Achchuthan Shanmugasundram Gene: btd has been classified as Amber List (Moderate Evidence).
Optic neuropathy v4.28 BTD Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: BTD.
Optic neuropathy v4.28 BTD Achchuthan Shanmugasundram gene: BTD was added
gene: BTD was added to Optic neuropathy. Sources: Literature
Mode of inheritance for gene: BTD was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: BTD were set to 26203071; 29025919; 32235217; 33364171
Phenotypes for gene: BTD were set to Biotinidase deficiency, OMIM:253260
Review for gene: BTD was set to GREEN
Added comment: PMID:26203071 - A 22-year-old man presented with a disabling extensive myelopathy and bilateral optic neuropathy which mimicked the findings of a (seronegative) neuromyelitis optica. A novel homozygous BTD variant (p.Ala439Asp) and a known variant (c.1413T>C/ p.Cys471Cys) were identified in this patient.

PMID:29025919 - Two unrelated individuals with adult-onset biotinidase deficiency had severe, but reversible optic neuropathy. They were identified with compound heterozygous variants (patient 1: p.Phe232Cys/ p.Leu440Pro; patient 2: p.Gln456His/ p.Arg538Cys).

PMID:32235217 - A 49-year-old man was reported with progressive optic atrophy, peripheral neuropathy, and systemic weakness and fatigue due to biotinidase deficiency. This patient was reported with compound heterozygous variants (p.Ala171Thr/ p.Asp444His)

PMID:33364171 - Two adult brothers were reported with biallelic BTD variants. Both of them presented with lower limb neuropathy and one had progressive optic neuropathy.
Sources: Literature
Possible mitochondrial disorder - nuclear genes v3.105 SLIRP Achchuthan Shanmugasundram Classified gene: SLIRP as Red List (low evidence)
Possible mitochondrial disorder - nuclear genes v3.105 SLIRP Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Zornitza Stark, there is one case with compound heterozygous SLIRP variants and the gene should be rated red.
Possible mitochondrial disorder - nuclear genes v3.105 SLIRP Achchuthan Shanmugasundram Gene: slirp has been classified as Red List (Low Evidence).
Possible mitochondrial disorder - nuclear genes v3.104 SLIRP Achchuthan Shanmugasundram reviewed gene: SLIRP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cerebral vascular malformations v3.15 COL5A1 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: COL5A1.
Cerebral vascular malformations v3.15 COL5A1 Achchuthan Shanmugasundram Classified gene: COL5A1 as Amber List (moderate evidence)
Cerebral vascular malformations v3.15 COL5A1 Achchuthan Shanmugasundram Gene: col5a1 has been classified as Amber List (Moderate Evidence).
Cerebral vascular malformations v3.14 COL5A1 Achchuthan Shanmugasundram Added comment: Comment on mode of inheritance: There is sufficient evidence available for the association of heterozygous COL5A1 variants with this panel. However, there are only two cases reported with compound heterozygous variants. Hence the MOI should be set as 'MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted'.
Cerebral vascular malformations v3.14 COL5A1 Achchuthan Shanmugasundram Mode of inheritance for gene: COL5A1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral vascular malformations v3.13 COL5A1 Achchuthan Shanmugasundram Phenotypes for gene: COL5A1 were changed from Fibromuscular dysplasia, multifocal to Ehlers-Danlos syndrome, classic type, 1, OMIM:130000; Fibromuscular dysplasia, multifocal, OMIM:619329
Cerebral vascular malformations v3.12 COL5A1 Achchuthan Shanmugasundram Publications for gene: COL5A1 were set to PMID: 32938213
Cerebral vascular malformations v3.11 COL5A1 Achchuthan Shanmugasundram edited their review of gene: COL5A1: Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral vascular malformations v3.11 COL5A1 Achchuthan Shanmugasundram edited their review of gene: COL5A1: Changed phenotypes to: Ehlers-Danlos syndrome, classic type, 1, OMIM:130000, Fibromuscular dysplasia, multifocal, OMIM:619329
Cerebral vascular malformations v3.11 COL5A1 Achchuthan Shanmugasundram changed review comment from: PMID:17053184 - Of 15 patients from seven families with spontaneous cervical artery dissections (CAD) recruited in this study, two patients from a family carried a rare variant in COL5A1 (p.Asp192Asn). One of them also carried a rare variant in COL5A2.

PMID:31903434 - Among 43 patients with cervical artery dissection (CeAD) analysed in this study, one patient had classic Ehlers Danlos syndrome due to two different missense variants in COL5A1 (p.Arg65Trp and p.Val172Phe), while another patient had missense variants in COL5A2 (p.Pro1103Leu) and COL5A1 (p.Thr1757Met).

PMID:32938213 - Four unrelated individuals were reported with the same heterozygous variant in COL5A1 (p.Gly514Ser) and they presented with arterial aneurysms, dissections, tortuosity, and mFMD affecting multiple arteries. The existence of a common haplotype among all four probands suggest founder effect.

PMID:33189937 - A 22-year-old patient with intracranial aneurysm and mild connective tissue manifestations reminiscent of EDS was identified with two COL5A1 missense variants in trans configuration (p.Gly530Ser and p.Pro1379Ser).

PMID:35911880; to: PMID:17053184 - Of 15 patients from seven families with spontaneous cervical artery dissections (CAD) recruited in this study, two patients from a family carried a rare variant in COL5A1 (p.Asp192Asn). One of them also carried a rare variant in COL5A2.

PMID:31903434 - Among 43 patients with cervical artery dissection (CeAD) analysed in this study, one patient had classic Ehlers Danlos syndrome due to two different missense variants in COL5A1 (p.Arg65Trp and p.Val172Phe), while another patient had missense variants in COL5A2 (p.Pro1103Leu) and COL5A1 (p.Thr1757Met).

PMID:32938213 - Four unrelated individuals were reported with the same heterozygous variant in COL5A1 (p.Gly514Ser) and they presented with arterial aneurysms, dissections, tortuosity, and mFMD affecting multiple arteries. The existence of a common haplotype among all four probands suggest founder effect.

PMID:33189937 - A 22-year-old patient with intracranial aneurysm and mild connective tissue manifestations reminiscent of EDS was identified with two COL5A1 missense variants in trans configuration (p.Gly530Ser and p.Pro1379Ser).

PMID:35911880 - A female was reported with postpartum arterial dissection involving all four cervicocephalic arteries resulting in acute cerebral infarction. She was identified with a heterozygous COL5A1 gene variant (p.Asp1648Gly).

This gene has been associated with relevant phenotypes in OMIM and Gene2Phenotype.
Cerebral vascular malformations v3.11 COL5A1 Achchuthan Shanmugasundram reviewed gene: COL5A1: Rating: AMBER; Mode of pathogenicity: None; Publications: 17053184, 31903434, 32938213, 33189937, 35911880; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Monogenic hearing loss v4.36 GRAP Achchuthan Shanmugasundram commented on gene: GRAP: As reviewed by Barbara Vona, two unrelated families were reported with the same homozygous missense variant. There is some functional data available as well.

This gene has been associated with relevant phenotype in OMIM (MIM #618456).
Monogenic hearing loss v4.36 GRAP Achchuthan Shanmugasundram Classified gene: GRAP as Red List (low evidence)
Monogenic hearing loss v4.36 GRAP Achchuthan Shanmugasundram Gene: grap has been classified as Red List (Low Evidence).
Monogenic hearing loss v4.35 GRAP Achchuthan Shanmugasundram Phenotypes for gene: GRAP were changed from Non-syndromic hearing loss to Deafness, autosomal recessive 114, OMIM:618456
Monogenic hearing loss v4.34 GRAP Achchuthan Shanmugasundram reviewed gene: GRAP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 114, OMIM:618456; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Monogenic hearing loss v4.34 GRAP Achchuthan Shanmugasundram Publications for gene: GRAP were set to PMID: 30610177
Proteinuric renal disease v4.12 RCAN1 Achchuthan Shanmugasundram commented on gene: RCAN1: As reviewed by Zornitza Stark, whole-genome sequencing performed on 320 individuals from 201 families with familial and sporadic nephrotic syndrome (NS)/ focal segmental glomerulosclerosis (FSGS) identified two variants in RCAN1 gene in two families with autosomal dominant FSGS/ steroid-resistant nephrotic syndrome (SRNS). In addition, there is some functional data available.

This gene has not been associated with any phenotypes either in OMIM or in Gene2Phenotype.

This gene can be rated amber with current evidence.
Proteinuric renal disease v4.12 RCAN1 Achchuthan Shanmugasundram Classified gene: RCAN1 as Amber List (moderate evidence)
Proteinuric renal disease v4.12 RCAN1 Achchuthan Shanmugasundram Gene: rcan1 has been classified as Amber List (Moderate Evidence).
Proteinuric renal disease v4.11 RCAN1 Achchuthan Shanmugasundram Phenotypes for gene: RCAN1 were changed from FSGS; proteinuria to focal segmental glomerulosclerosis, MONDO:0100313; nephrotic syndrome, MONDO:0005377
Proteinuric renal disease v4.10 RCAN1 Achchuthan Shanmugasundram reviewed gene: RCAN1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: focal segmental glomerulosclerosis, MONDO:0100313, nephrotic syndrome, MONDO:0005377; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Proteinuric renal disease v4.10 PRDM15 Achchuthan Shanmugasundram Classified gene: PRDM15 as Amber List (moderate evidence)
Proteinuric renal disease v4.10 PRDM15 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available (six unrelated individuals with three different biallelic variants, mouse and Xenopus models and functional data) for the promotion of this gene to green rating in the next GMS update.
Proteinuric renal disease v4.10 PRDM15 Achchuthan Shanmugasundram Gene: prdm15 has been classified as Amber List (Moderate Evidence).
Proteinuric renal disease v4.9 PRDM15 Achchuthan Shanmugasundram Phenotypes for gene: PRDM15 were changed from Steroid resistant nephrotic syndrome; Holoprosencephaly to steroid-resistant nephrotic syndrome, MONDO:0044765
Proteinuric renal disease v4.8 PRDM15 Achchuthan Shanmugasundram Publications for gene: PRDM15 were set to 31950080
Proteinuric renal disease v4.7 PRDM15 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: PRDM15.
Proteinuric renal disease v4.7 PRDM15 Achchuthan Shanmugasundram reviewed gene: PRDM15: Rating: GREEN; Mode of pathogenicity: None; Publications: 33593823; Phenotypes: steroid-resistant nephrotic syndrome, MONDO:0044765; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Optic neuropathy v4.27 PDXK Achchuthan Shanmugasundram Classified gene: PDXK as Amber List (moderate evidence)
Optic neuropathy v4.27 PDXK Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available (three unrelated cases and functional studies) for the promotion of this gene to green rating in the next GMS update.
Optic neuropathy v4.27 PDXK Achchuthan Shanmugasundram Gene: pdxk has been classified as Amber List (Moderate Evidence).
Optic neuropathy v4.26 PDXK Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: PDXK.
Hereditary neuropathy or pain disorder v3.87 PDXK Achchuthan Shanmugasundram Classified gene: PDXK as Amber List (moderate evidence)
Hereditary neuropathy or pain disorder v3.87 PDXK Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available (three unrelated cases and functional studies) for the promotion of this gene to green rating in the next GMS update.
Hereditary neuropathy or pain disorder v3.87 PDXK Achchuthan Shanmugasundram Gene: pdxk has been classified as Amber List (Moderate Evidence).
Hereditary neuropathy or pain disorder v3.86 PDXK Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: PDXK.
Optic neuropathy v4.26 PDXK Achchuthan Shanmugasundram gene: PDXK was added
gene: PDXK was added to Optic neuropathy. Sources: Literature
Mode of inheritance for gene: PDXK was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PDXK were set to 31187503; 32522499
Phenotypes for gene: PDXK were set to Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy, OMIM:618511
Review for gene: PDXK was set to GREEN
Added comment: PMID:31187503 - Five individuals from two unrelated families were reported with biallelic PDXK variants and with primary axonal polyneuropathy and optic atrophy. This association was also supported by results from cell-based functional assays. The biochemical profile can be rescued with PLP supplementation associated with clinical improvement.

PMID:32522499 - Two affected siblings with a novel biallelic missense PDXK variant were reported with a similar phenotype as reported in PMID:31187503 with earlier onset. Functional analysis showed that this variant leads to almost complete loss of PDXK enzymatic activity and low PLP levels.

This gene has been associated with relevant phenotypes in OMIM (MIM #618511), but not yet in Gene2Phenotype.
Sources: Literature
Hereditary neuropathy or pain disorder v3.86 PDXK Achchuthan Shanmugasundram gene: PDXK was added
gene: PDXK was added to Hereditary neuropathy or pain disorder. Sources: Literature
Mode of inheritance for gene: PDXK was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PDXK were set to 31187503; 32522499
Phenotypes for gene: PDXK were set to Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy, OMIM:618511
Review for gene: PDXK was set to GREEN
Added comment: PMID:31187503 - Five individuals from two unrelated families were reported with biallelic PDXK variants and with primary axonal polyneuropathy and optic atrophy. This association was also supported by results from cell-based functional assays. The biochemical profile can be rescued with PLP supplementation associated with clinical improvement.

PMID:32522499 - Two affected siblings with a novel biallelic missense PDXK variant were reported with a similar phenotype as reported in PMID:31187503 with earlier onset. Functional analysis showed that this variant leads to almost complete loss of PDXK enzymatic activity and low PLP levels.

This gene has been associated with relevant phenotypes in OMIM (MIM #618511), but not yet in Gene2Phenotype.
Sources: Literature
Fetal anomalies v3.149 NRXN2 Sarah Leigh Publications for gene: NRXN2 were set to
Fetal hydrops v1.64 FZD6 Irina Adamena gene: FZD6 was added
gene: FZD6 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: FZD6 was set to Unknown
Publications for gene: FZD6 were set to PMID: 33082562
Phenotypes for gene: FZD6 were set to Nonimmune hydrops fetalis
Review for gene: FZD6 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 GLMN Irina Adamena gene: GLMN was added
gene: GLMN was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: GLMN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GLMN were set to PMID: 33082562
Phenotypes for gene: GLMN were set to Nonimmune hydrops fetalis
Review for gene: GLMN was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 ITGA9 Irina Adamena gene: ITGA9 was added
gene: ITGA9 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: ITGA9 was set to Unknown
Publications for gene: ITGA9 were set to PMID: 33082562
Phenotypes for gene: ITGA9 were set to Nonimmune hydrops fetalis
Review for gene: ITGA9 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Hereditary neuropathy or pain disorder v3.84 SPG7 Sarah Leigh changed review comment from: SPG7 variants have been associated with Spastic paraplegia 7, autosomal recessive (OMIM:607259) and have a definitive association with the same condition on the Eye panel at Gen2Phen. Various phenotypic features are apparent in cases of OMIM:607259. Peripheral neuropathy has been reported in at least three cases (PMID: 35096021, in the review on this panel by Williams Kirsty), and optical neuropathy has been reported in many more cases (as mentioned in PMID:35243150).; to: SPG7 variants have been associated with Spastic paraplegia 7, autosomal recessive (OMIM:607259) and have a definitive association with the same condition on the Eye panel at Gen2Phen. Various phenotypic features are apparent in cases of OMIM:607259. Peripheral neuropathy has been reported in at least three cases (PMID: 35096021, in the review on this panel by Kirsty Williams), and optical neuropathy has been reported in many more cases (as mentioned in PMID:35243150).
Fetal hydrops v1.64 CANT1 Irina Adamena gene: CANT1 was added
gene: CANT1 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: CANT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CANT1 were set to PMID: 33082562
Phenotypes for gene: CANT1 were set to Nonimmune hydrops fetalis
Review for gene: CANT1 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 PTH1R Irina Adamena reviewed gene: PTH1R: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 GPI Irina Adamena gene: GPI was added
gene: GPI was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: GPI was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GPI were set to PMID: 33082562
Phenotypes for gene: GPI were set to Nonimmune hydrops fetalis
Review for gene: GPI was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 G6PD Irina Adamena gene: G6PD was added
gene: G6PD was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: G6PD was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: G6PD were set to PMID: 33082562
Phenotypes for gene: G6PD were set to Nonimmune hydrops fetalis
Review for gene: G6PD was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 RPL15 Irina Adamena gene: RPL15 was added
gene: RPL15 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: RPL15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPL15 were set to PMID: 33082562
Phenotypes for gene: RPL15 were set to Nonimmune hydrops fetalis
Review for gene: RPL15 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 PRF1 Irina Adamena gene: PRF1 was added
gene: PRF1 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: PRF1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PRF1 were set to PMID: 33082562
Phenotypes for gene: PRF1 were set to Nonimmune hydrops fetalis
Review for gene: PRF1 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 GATA1 Irina Adamena reviewed gene: GATA1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Fetal hydrops v1.64 SEC23B Irina Adamena gene: SEC23B was added
gene: SEC23B was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: SEC23B was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SEC23B were set to PMID: 33082562
Phenotypes for gene: SEC23B were set to Nonimmune hydrops fetalis
Review for gene: SEC23B was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 CDAN1 Irina Adamena reviewed gene: CDAN1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 SPTB Irina Adamena gene: SPTB was added
gene: SPTB was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: SPTB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SPTB were set to PMID: 33082562
Phenotypes for gene: SPTB were set to Nonimmune hydrops fetalis
Review for gene: SPTB was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 SLC4A1 Irina Adamena gene: SLC4A1 was added
gene: SLC4A1 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: SLC4A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SLC4A1 were set to PMID: 33082562
Phenotypes for gene: SLC4A1 were set to Nonimmune hydrops fetalis
Review for gene: SLC4A1 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 SGPL1 Irina Adamena reviewed gene: SGPL1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 GBE1 Irina Adamena reviewed gene: GBE1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 MT-TL1 Irina Adamena gene: MT-TL1 was added
gene: MT-TL1 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene gene: MT-TL1 was set to MITOCHONDRIAL
Publications for gene: MT-TL1 were set to PMID: 33082562
Phenotypes for gene: MT-TL1 were set to Nonimmune hydrops fetalis
Review for gene: MT-TL1 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 MT-TE Irina Adamena gene: MT-TE was added
gene: MT-TE was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene gene: MT-TE was set to MITOCHONDRIAL
Publications for gene: MT-TE were set to PMID: 33082562
Phenotypes for gene: MT-TE were set to Nonimmune hydrops fetalis
Review for gene: MT-TE was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 MVK Irina Adamena reviewed gene: MVK: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 MGAT2 Irina Adamena gene: MGAT2 was added
gene: MGAT2 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: MGAT2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MGAT2 were set to PMID: 33082562
Phenotypes for gene: MGAT2 were set to Nonimmune hydrops fetalis
Review for gene: MGAT2 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 SLC17A5 Irina Adamena reviewed gene: SLC17A5: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 GLB1 Irina Adamena reviewed gene: GLB1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 GUSB Irina Adamena reviewed gene: GUSB: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 GALNS Irina Adamena reviewed gene: GALNS: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33082562; Phenotypes: Nonimmune hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 SCN5A Irina Adamena gene: SCN5A was added
gene: SCN5A was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: SCN5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SCN5A were set to PMID: 33082562
Phenotypes for gene: SCN5A were set to Nonimmune hydrops fetalis
Review for gene: SCN5A was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 KCNH2 Irina Adamena gene: KCNH2 was added
gene: KCNH2 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: KCNH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KCNH2 were set to PMID: 33082562
Phenotypes for gene: KCNH2 were set to Nonimmune hydrops fetalis
Review for gene: KCNH2 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 ALPK3 Irina Adamena gene: ALPK3 was added
gene: ALPK3 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: ALPK3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ALPK3 were set to PMID: 33082562
Phenotypes for gene: ALPK3 were set to Nonimmune hydrops fetalis
Review for gene: ALPK3 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 MYH7 Irina Adamena gene: MYH7 was added
gene: MYH7 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: MYH7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MYH7 were set to PMID: 33082562
Phenotypes for gene: MYH7 were set to Nonimmune hydrops fetalis
Review for gene: MYH7 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 LAMB2 Irina Adamena gene: LAMB2 was added
gene: LAMB2 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: LAMB2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LAMB2 were set to PMID: 33082562
Phenotypes for gene: LAMB2 were set to Nonimmune hydrops fetalis
Review for gene: LAMB2 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
White matter disorders and cerebral calcification - narrow panel v3.34 NAA60 Sarah Leigh Classified gene: NAA60 as Amber List (moderate evidence)
White matter disorders and cerebral calcification - narrow panel v3.34 NAA60 Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
White matter disorders and cerebral calcification - narrow panel v3.34 NAA60 Sarah Leigh Gene: naa60 has been classified as Amber List (Moderate Evidence).
White matter disorders and cerebral calcification - narrow panel v3.33 NAA60 Sarah Leigh gene: NAA60 was added
gene: NAA60 was added to White matter disorders and cerebral calcification - narrow panel. Sources: Literature
Q2_24_promote_green, Q2_24_NHS_review tags were added to gene: NAA60.
Mode of inheritance for gene: NAA60 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: NAA60 were set to 38480682
Phenotypes for gene: NAA60 were set to NAA60 associated autosomal recessive primary familial brain calcifications
Review for gene: NAA60 was set to GREEN
Added comment: To date, NAA60 variants are not associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38480682 reports six NAA60 variants in six unrelated cases with an autosomal recessive primary familial brain calcification (PFBC). Table 2 in PMID: 38480682 outlines the extent of the calcification seen in the patient's CT scans. Functional studies show that the phosphate importer SLC20A2 is a substrate of NAA60 in vitro, and loss of function by the NAA60 variants results in a reduced level of surface SLC20A2, thereby, reducing the extracellular phosphate uptake. The authors conclude, that this study provides a possible biochemical explanation of the involvement of NAA60 variants in PFBC development (PMID: 38480682).
Sources: Literature
Fetal hydrops v1.64 CDC42 Irina Adamena gene: CDC42 was added
gene: CDC42 was added to Fetal hydrops. Sources: Literature
Mode of inheritance for gene: CDC42 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CDC42 were set to PMID: 33082562
Phenotypes for gene: CDC42 were set to Nonimmune hydrops fetalis
Review for gene: CDC42 was set to GREEN
Added comment: Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: Literature
Fetal hydrops v1.64 SLC30A5 Irina Adamena changed review comment from: Four affected children with homozygous loss of function variants in SLC30A5 gene with cardiomyopathy, hydrops fetalis, or cystic hygroma.; to: Four affected children with homozygous loss of function variants in SLC30A5 gene with cardiomyopathy, hydrops fetalis, or cystic hygroma (PMID: 33547425).
Fetal hydrops v1.64 ANGPT2 Irina Adamena reviewed gene: ANGPT2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 34876502; Phenotypes: Hydrops fetalis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal hydrops v1.64 SLC30A5 Irina Adamena reviewed gene: SLC30A5: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33547425; Phenotypes: hydrops fetalis, cardiomyopathy, cystic hygroma; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Monogenic hearing loss v4.33 NLRP12 Achchuthan Shanmugasundram Classified gene: NLRP12 as Amber List (moderate evidence)
Monogenic hearing loss v4.33 NLRP12 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available (three unrelated cases) for the association of NLRP12 with sensorineural hearing loss and hence this gene can be promoted to green rating in the next GMS review.
Monogenic hearing loss v4.33 NLRP12 Achchuthan Shanmugasundram Gene: nlrp12 has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v4.32 NLRP12 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: NLRP12.
Monogenic hearing loss v4.32 NLRP12 Achchuthan Shanmugasundram changed review comment from: PMID:18230725 - Two unrelated families from Guadeloupe were reported with a periodic fever syndrome and with monoallelic NLRP12 variants. Of these, twin boys from family 1 had bilateral sensorineural hearing loss.

PMID:24064030 - Six unrelated Italian patients were reported with familial cold autoinflammatory syndrome 2 and NLRP12 variants, of which one patient had sensorineural hearing loss.

PMID:31820221 - Three cases presenting with NLRP12 - autoinflammatory disorder were reported, where one had sensorineural deafness.
Sources: Literature; to: PMID:18230725 - Two unrelated families from Guadeloupe were reported with a periodic fever syndrome and with monoallelic NLRP12 variants. Of these, twin boys from family 1 had bilateral sensorineural hearing loss.

PMID:24064030 - Six unrelated Italian patients were reported with familial cold autoinflammatory syndrome 2 and NLRP12 variants, of which one patient had sensorineural hearing loss.

PMID:31820221 - Three cases presenting with NLRP12 - autoinflammatory disorder were reported, where one had sensorineural deafness.

NLRP12 has been associated with Familial cold autoinflammatory syndrome 2 (MIM #611762) in OMIM and sensorineural deafness has been listed as one of the clinical presentations of this phenotype.

Sources: Literature
Monogenic hearing loss v4.32 NLRP12 Achchuthan Shanmugasundram gene: NLRP12 was added
gene: NLRP12 was added to Monogenic hearing loss. Sources: Literature
Mode of inheritance for gene: NLRP12 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NLRP12 were set to 18230725; 24064030; 31820221
Phenotypes for gene: NLRP12 were set to Familial cold autoinflammatory syndrome 2, OMIM:611762; sensorineural hearing loss disorder, MONDO:0020678
Review for gene: NLRP12 was set to GREEN
Added comment: PMID:18230725 - Two unrelated families from Guadeloupe were reported with a periodic fever syndrome and with monoallelic NLRP12 variants. Of these, twin boys from family 1 had bilateral sensorineural hearing loss.

PMID:24064030 - Six unrelated Italian patients were reported with familial cold autoinflammatory syndrome 2 and NLRP12 variants, of which one patient had sensorineural hearing loss.

PMID:31820221 - Three cases presenting with NLRP12 - autoinflammatory disorder were reported, where one had sensorineural deafness.
Sources: Literature
Childhood solid tumours v4.18 KDM3B Achchuthan Shanmugasundram Classified gene: KDM3B as Amber List (moderate evidence)
Childhood solid tumours v4.18 KDM3B Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Dmitrijs Rots, there are four cases reported with KDM3B variants and with cancer, of which three cases are childhood solid tumours (two cases with Wilms tumour and one case with Hodgkin lymphoma), while the fourth case had acute myeloid leukaemia in childhood.

Hence, this gene can be promoted to green rating in the next GMS review.
Childhood solid tumours v4.18 KDM3B Achchuthan Shanmugasundram Gene: kdm3b has been classified as Amber List (Moderate Evidence).
Childhood solid tumours v4.17 KDM3B Achchuthan Shanmugasundram Phenotypes for gene: KDM3B were changed from Diets-Jongmans syndrome to Diets-Jongmans syndrome, OMIM:618846
Childhood solid tumours v4.16 KDM3B Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: KDM3B.
Childhood solid tumours v4.16 KDM3B Achchuthan Shanmugasundram reviewed gene: KDM3B: Rating: GREEN; Mode of pathogenicity: None; Publications: 30885698, 30929739; Phenotypes: Diets-Jongmans syndrome, OMIM:618846; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability v5.521 DENND5B Sarah Leigh Classified gene: DENND5B as Amber List (moderate evidence)
Intellectual disability v5.521 DENND5B Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Intellectual disability v5.521 DENND5B Sarah Leigh Gene: dennd5b has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.520 DENND5B Sarah Leigh Tag Q2_24_promote_green tag was added to gene: DENND5B.
Tag Q2_24_NHS_review tag was added to gene: DENND5B.
Early onset or syndromic epilepsy v4.193 DENND5B Sarah Leigh Classified gene: DENND5B as Amber List (moderate evidence)
Early onset or syndromic epilepsy v4.193 DENND5B Sarah Leigh Gene: dennd5b has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy v4.192 DENND5B Sarah Leigh edited their review of gene: DENND5B: Changed rating: AMBER
Early onset or syndromic epilepsy v4.192 DENND5B Sarah Leigh gene: DENND5B was added
gene: DENND5B was added to Early onset or syndromic epilepsy. Sources: Literature
Mode of inheritance for gene: DENND5B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: DENND5B were set to 38387458
Phenotypes for gene: DENND5B were set to DENND5B associated neurodevelopmental disorder
Review for gene: DENND5B was set to GREEN
Added comment: DENND5B variants have not previously been associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38387458 reports five de novo missense variants in five unrelated cases. The carriers of these DENND5B variants have a neurodevelopmental disorder, which is characterized by psychomotor delay (5/5 cases), intellectual disability, ranging from severe to mild (3/5 cases, although one of the negative cases was a 2 year old child, who was considered to be too young to make the assessment, although the DD/intellectual disability phenotype was considered to be moderate in this case), epilepsy (2/5 cases) and hypotonia (4/5 cases). The authors of PMID: 38387458 also report the functional effects of the DENND5B variants, which revealed defective intracellular vesicle trafficking, with significant impairment of lipid uptake and distribution. They conclude that this effect is likely to be caused by the predicted disruption of protein folding in the variant DENND5B peptide.
Sources: Literature
Intellectual disability v5.520 DENND5B Sarah Leigh gene: DENND5B was added
gene: DENND5B was added to Intellectual disability - microarray and sequencing. Sources: Literature
Mode of inheritance for gene: DENND5B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: DENND5B were set to 38387458
Phenotypes for gene: DENND5B were set to DENND5B associated neurodevelopmental disorder
Review for gene: DENND5B was set to GREEN
Added comment: DENND5B variants have not previously been associated with a phenotype in OMIM, Gen2Phen or MONDO. PMID: 38387458 reports five de novo missense variants in five unrelated cases. The carriers of these DENND5B variants have a neurodevelopmental disorder, which is characterized by psychomotor delay (5/5 cases), intellectual disability, ranging from severe to mild (3/5 cases, although one of the negative cases was a 2 year old child, who was considered to be too young to make the assessment, although the DD/intellectual disability phenotype was considered to be moderate in this case), epilepsy (2/5 cases) and hypotonia (4/5 cases). The authors of PMID: 38387458 also report the functional effects of the DENND5B variants, which revealed defective intracellular vesicle trafficking, with significant impairment of lipid uptake and distribution. They conclude that this effect is likely to be caused by the predicted disruption of protein folding in the variant DENND5B peptide.
Sources: Literature
Intellectual disability v5.519 TBC1D2B Sarah Leigh Tag watchlist was removed from gene: TBC1D2B.
Tag Q2_24_promote_green tag was added to gene: TBC1D2B.
Tag Q2_24_NHS_review tag was added to gene: TBC1D2B.
Intellectual disability v5.519 TBC1D2B Sarah Leigh Classified gene: TBC1D2B as Amber List (moderate evidence)
Intellectual disability v5.519 TBC1D2B Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Intellectual disability v5.519 TBC1D2B Sarah Leigh Gene: tbc1d2b has been classified as Amber List (Moderate Evidence).
Intellectual disability v5.518 TBC1D2B Sarah Leigh reviewed gene: TBC1D2B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Early onset or syndromic epilepsy v4.191 TBC1D2B Sarah Leigh edited their review of gene: TBC1D2B: Added comment: TBC1D2B variants have been associated with Neurodevelopmental disorder with seizures and gingival overgrowth (OMIM:619323) and as definitive Gen2Phen gene for TBC1D2B-related neurodevelopmental disorder. So far, 11 TBC1D2B variants have been reported in 8 unrelated families. Global developmental delay (HP:0001263) was reported in 5/8 families, mental deterioration (HP:0001268) was seen in 5/8 families and seizures (HP:0001250) were reported in 8/8 families (four of these were controlled with medication)(PMID: 38374468).; Changed rating: GREEN
Intellectual disability v5.518 TBC1D2B Sarah Leigh Publications for gene: TBC1D2B were set to 32623794
Early onset or syndromic epilepsy v4.191 TBC1D2B Sarah Leigh Publications for gene: TBC1D2B were set to 32623794
Intellectual disability v5.517 TBC1D2B Sarah Leigh Phenotypes for gene: TBC1D2B were changed from Global developmental delay; Intellectual disability; Seizures; Gingival overgrowth; Behavioral abnormality; Abnormality of the mandible; Abnormality of brain morphology; Abnormality of the eye; Hearing abnormality to Neurodevelopmental disorder with seizures and gingival overgrowth, OMIM:619323; neurodevelopmental disorder with seizures and gingival overgrowth, MONDO:0859148
Early onset or syndromic epilepsy v4.190 TBC1D2B Sarah Leigh Phenotypes for gene: TBC1D2B were changed from Global developmental delay; Intellectual disability; Seizures; Gingival overgrowth; Behavioral abnormality; Abnormality of the mandible; Abnormality of brain morphology; Abnormality of the eye; Hearing abnormality to Neurodevelopmental disorder with seizures and gingival overgrowth, OMIM:619323; neurodevelopmental disorder with seizures and gingival overgrowth, MONDO:0859148
Ichthyosis and erythrokeratoderma v3.28 DBR1 Achchuthan Shanmugasundram Classified gene: DBR1 as Amber List (moderate evidence)
Ichthyosis and erythrokeratoderma v3.28 DBR1 Achchuthan Shanmugasundram Gene: dbr1 has been classified as Amber List (Moderate Evidence).
Ichthyosis and erythrokeratoderma v3.27 DBR1 Achchuthan Shanmugasundram Tag founder-effect tag was added to gene: DBR1.
Ichthyosis and erythrokeratoderma v3.27 DBR1 Achchuthan Shanmugasundram changed review comment from: Comment on list classification: As reviewed by Zornitza Stark, the same variant was identified in four different families and haplotype analysis suggests this to be a founder variant.; to: Comment on list classification: As reviewed by Zornitza Stark, the same variant was identified in four different families and haplotype analysis suggests this to be a founder variant. There is functional data available. This gene can only be rated amber with the current evidence.

The 'founder-effect' tag is added to this gene.
Ichthyosis and erythrokeratoderma v3.27 DBR1 Achchuthan Shanmugasundram Classified gene: DBR1 as No list
Ichthyosis and erythrokeratoderma v3.27 DBR1 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Zornitza Stark, the same variant was identified in four different families and haplotype analysis suggests this to be a founder variant.
Ichthyosis and erythrokeratoderma v3.27 DBR1 Achchuthan Shanmugasundram Gene: dbr1 has been removed from the panel.
Ichthyosis and erythrokeratoderma v3.26 DBR1 Achchuthan Shanmugasundram edited their review of gene: DBR1: Changed phenotypes to: ichthyosis, MONDO:0019269
Ichthyosis and erythrokeratoderma v3.26 DBR1 Achchuthan Shanmugasundram Phenotypes for gene: DBR1 were changed from Ichthyosis (MONDO#0019269), DBR1-related to ichthyosis, MONDO:0019269
Ichthyosis and erythrokeratoderma v3.25 DBR1 Achchuthan Shanmugasundram reviewed gene: DBR1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: inherited ichthyosis, MONDO:0015947; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ehlers Danlos syndrome with a likely monogenic cause v3.12 ADAMTSL2 Achchuthan Shanmugasundram Classified gene: ADAMTSL2 as Amber List (moderate evidence)
Ehlers Danlos syndrome with a likely monogenic cause v3.12 ADAMTSL2 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Zornitza Stark, six families were reported with the same monoallelic variant and with Ehlers-Danlos syndrome. However, there is no functional data and it is not clear whether it is a founder variant. Hence, this gene can only be rated amber with the current evidence in this panel.
Ehlers Danlos syndrome with a likely monogenic cause v3.12 ADAMTSL2 Achchuthan Shanmugasundram Gene: adamtsl2 has been classified as Amber List (Moderate Evidence).
Ehlers Danlos syndrome with a likely monogenic cause v3.11 ADAMTSL2 Achchuthan Shanmugasundram reviewed gene: ADAMTSL2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Ehlers-Danlos syndrome, MONDO:0020066; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital adrenal hypoplasia v3.11 KDM1A Achchuthan Shanmugasundram Phenotypes for gene: KDM1A were changed from Food-dependent Cushing syndrome (FDCS) to Cleft palate, psychomotor retardation, and distinctive facial features, OMIM:616728; congenital adrenal hyperplasia, MONDO:0018479
Congenital adrenal hypoplasia v3.10 KDM1A Achchuthan Shanmugasundram Classified gene: KDM1A as Red List (low evidence)
Congenital adrenal hypoplasia v3.10 KDM1A Achchuthan Shanmugasundram Gene: kdm1a has been classified as Red List (Low Evidence).
Congenital adrenal hypoplasia v3.9 KDM1A Achchuthan Shanmugasundram reviewed gene: KDM1A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cleft palate, psychomotor retardation, and distinctive facial features, OMIM:616728, congenital adrenal hyperplasia, MONDO:0018479; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Rare genetic inflammatory skin disorders v3.10 GNB1 Achchuthan Shanmugasundram Classified gene: GNB1 as Amber List (moderate evidence)
Rare genetic inflammatory skin disorders v3.10 GNB1 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Dmitrijs Rots, there are five cases reported with cutaneous mastocytosis.

Cutaneous mastocytosis has also been reported as one of the clinical presentations of the OMIM phenotype Intellectual developmental disorder, autosomal dominant 42 (MIM #616973).

Hence, this gene can be promoted to green rating in the next GMS review.
Rare genetic inflammatory skin disorders v3.10 GNB1 Achchuthan Shanmugasundram Gene: gnb1 has been classified as Amber List (Moderate Evidence).
Rare genetic inflammatory skin disorders v3.9 GNB1 Achchuthan Shanmugasundram Phenotypes for gene: GNB1 were changed from Cutaneous mastocytosis; Intellectual developmental disorder, autosomal dominant 42 to Intellectual developmental disorder, autosomal dominant 42, OMIM:616973; cutaneous mastocytosis, MONDO:0019023
Rare genetic inflammatory skin disorders v3.8 GNB1 Achchuthan Shanmugasundram Publications for gene: GNB1 were set to 35119134
Rare genetic inflammatory skin disorders v3.7 GNB1 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: GNB1.
Rare genetic inflammatory skin disorders v3.7 GNB1 Achchuthan Shanmugasundram reviewed gene: GNB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29174093, 30194818, 35119134; Phenotypes: Intellectual developmental disorder, autosomal dominant 42, OMIM:616973, cutaneous mastocytosis, MONDO:0019023; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Thoracic aortic aneurysm or dissection (GMS) v3.11 SECISBP2 Achchuthan Shanmugasundram Tag Q2_24_NHS_review tag was added to gene: SECISBP2.
Thoracic aortic aneurysm or dissection (GMS) v3.11 SECISBP2 Achchuthan Shanmugasundram Classified gene: SECISBP2 as Amber List (moderate evidence)
Thoracic aortic aneurysm or dissection (GMS) v3.11 SECISBP2 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available (four unrelated cases and animal models) for the promotion of this gene to green rating in the next GMS review.
Thoracic aortic aneurysm or dissection (GMS) v3.11 SECISBP2 Achchuthan Shanmugasundram Gene: secisbp2 has been classified as Amber List (Moderate Evidence).
Thoracic aortic aneurysm or dissection (GMS) v3.10 SECISBP2 Achchuthan Shanmugasundram Phenotypes for gene: SECISBP2 were changed from Growth retardation; sensorineural hearing loss; muscular dystrophy; thoracic aortic aneurysm; raised circulating thyroxine and low plasma selenium to Thyroid hormone metabolism, abnormal, 1, OMIM:609698; thoracic aortic aneurysm
Thoracic aortic aneurysm or dissection (GMS) v3.9 SECISBP2 Achchuthan Shanmugasundram Publications for gene: SECISBP2 were set to PMID 38042913; PMID 21084748
Thoracic aortic aneurysm or dissection (GMS) v3.8 SECISBP2 Achchuthan Shanmugasundram Tag Q2_24_promote_green tag was added to gene: SECISBP2.
Thoracic aortic aneurysm or dissection (GMS) v3.8 SECISBP2 Achchuthan Shanmugasundram reviewed gene: SECISBP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 38042913; Phenotypes: Thyroid hormone metabolism, abnormal, 1, OMIM:609698; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v4.83 RP1L1 Arina Puzriakova Added comment: Comment on mode of inheritance: This gene is associated with occult macular dystrophy (monoallelic variants) and retinitis pigmentosa (biallelic variants) (https://omim.org/entry/608581) with sufficient cases reported for each phenotype. Currently the monoallelic phenotype is not represented on any GMS panels.

Following curation and consultation with the Genomics England clinical team, there was agreement that macular dystrophy is part of the phenotypic target for this panel. Based on previous reviews, it is not clear why the monoallelic MOI was overwritten and therefore this gene will be flagged for specialist review to determine whether the MOI should stay as 'biallelic' or be updated to 'both mono- and biallelic'.
Retinal disorders v4.83 RP1L1 Arina Puzriakova Mode of inheritance for gene: RP1L1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v4.82 RP1L1 Arina Puzriakova Tag Q2_24_MOI tag was added to gene: RP1L1.
Tag Q2_24_expert_review tag was added to gene: RP1L1.
Monogenic hearing loss v4.31 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.31 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.31 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.31 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.31 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.30 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051; 32631815
Monogenic hearing loss v4.30 RIPOR2 Achchuthan Shanmugasundram Publications for gene: RIPOR2 were set to 17150207; 24958875; 9055809; 9205841; 24958875; 27269051
Monogenic hearing loss v4.29 RIPOR2 Achchuthan Shanmugasundram Phenotypes for gene: RIPOR2 were changed from Deafness, autosomal dominant 21, OMIM:607017; ?Deafness, autosomal recessive 104, OMIM:616515 to Deafness, autosomal dominant 21, OMIM:607017; ?Deafness, autosomal recessive 104, OMIM:616515
Monogenic hearing loss v4.29 RIPOR2 Achchuthan Shanmugasundram Phenotypes for gene: RIPOR2 were changed from ?Deafness, autosomal recessive 104 , OMIM:616515 to Deafness, autosomal dominant 21, OMIM:607017; ?Deafness, autosomal recessive 104, OMIM:616515
Monogenic hearing loss v4.28 RIPOR2 Achchuthan Shanmugasundram Classified gene: RIPOR2 as Amber List (moderate evidence)
Monogenic hearing loss v4.28 RIPOR2 Achchuthan Shanmugasundram Added comment: Comment on list classification: Only one variant was reported with both monoallelic and biallelic inheritance. There is some functional data for both modes of inheritance. Although there are 12 unrelated cases reported with the same monoallelic variant, this variant was suggested to be founder variant. Hence, this gene can only be rated amber with the current evidence for both modes of inheritance.
Monogenic hearing loss v4.28 RIPOR2 Achchuthan Shanmugasundram Gene: ripor2 has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v4.27 RIPOR2 Achchuthan Shanmugasundram changed review comment from: Biallelic variants:
PMID:24958875 reported six affected members from a single Turkish family with a homozygous splice site variant in the RIPOR2 gene (c.102-1G-A) and with deafness. In addition, morpholino knockdown of the orthologous gene in zebrafish embryos resulted in a significant reduction in the number of saccular hair cells and neuromasts, and caused hearing loss.

Monoallelic variants:
PMID:32631815 reported a heterozygous 12 nucleotide in-frame deletion (c.1696_1707del, p.Gln566_Lys569del) in RIPOR2 that was detected in 12 families of Dutch origin with non-syndromic hearing loss.

In total, the variant was detected in 59/63 affected participants, but also in five unaffected subjects from three family. Age of onset was highly variable, from congenital to 70 years (mean age: 30.6 years) - unaffected family members who harboured the variant were aged 23, 40, 49, 50, and 51 years, respectively. The authors speculated that the four affected subjects without the variant represent phenocopies. The presence of an identical variant in 12 families of common origin, as well as haplotype analysis, indicates a founder effect.

Functional analysis of this variant showed aberrant localisation of RIPOR2 variant protein in early postnatal mouse hair cells, ex vivo; and failure to rescue the stereocilia defects of Ripor2 knockout mice, in contrast to the rescue effect observed in cells expressing wild-type RIPOR2.; to: Biallelic variants:
PMID:24958875 reported six affected members from a single Turkish family with a homozygous splice site variant in the RIPOR2 gene (c.102-1G-A) and with deafness. In addition, morpholino knockdown of the orthologous gene in zebrafish embryos resulted in a significant reduction in the number of saccular hair cells and neuromasts, and caused hearing loss.

Monoallelic variants:
PMID:32631815 reported a heterozygous 12 nucleotide in-frame deletion (c.1696_1707del, p.Gln566_Lys569del) in RIPOR2 that was detected in 12 families of Dutch origin with non-syndromic hearing loss.

In total, the variant was detected in 59/63 affected participants, but also in five unaffected subjects from three family. Age of onset was highly variable, from congenital to 70 years (mean age: 30.6 years) - unaffected family members who harboured the variant were aged 23, 40, 49, 50, and 51 years, respectively. The authors speculated that the four affected subjects without the variant represent phenocopies. The presence of an identical variant in 12 families of common origin, as well as haplotype analysis, indicates a founder effect. Hence, the 'founder-effect' tag was added.

Functional analysis of this variant showed aberrant localisation of RIPOR2 variant protein in early postnatal mouse hair cells, ex vivo; and failure to rescue the stereocilia defects of Ripor2 knockout mice, in contrast to the rescue effect observed in cells expressing wild-type RIPOR2.
Monogenic hearing loss v4.27 RIPOR2 Achchuthan Shanmugasundram edited their review of gene: RIPOR2: Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Monogenic hearing loss v4.27 RIPOR2 Achchuthan Shanmugasundram Tag founder-effect tag was added to gene: RIPOR2.
Monogenic hearing loss v4.27 RIPOR2 Achchuthan Shanmugasundram reviewed gene: RIPOR2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24958875, 32631815; Phenotypes: Deafness, autosomal dominant 21, OMIM:607017, ?Deafness, autosomal recessive 104, OMIM:616515; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Severe Paediatric Disorders v1.184 CNTNAP2 Tracy Lester reviewed gene: CNTNAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital muscular dystrophy and congenital myopathy v0.226 MSTO1 Eleanor Williams commented on gene: MSTO1
Congenital muscular dystrophy and congenital myopathy v0.226 MSTO1 Eleanor Williams Tag Q2_24_MOI tag was added to gene: MSTO1.
Congenital muscular dystrophy and congenital myopathy v0.226 MSTO1 Eleanor Williams Mode of inheritance for gene: MSTO1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Intellectual disability v5.515 ASCC3 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Intellectual developmental disorder, autosomal recessive 81, OMIM:620700)
Intellectual disability v5.515 ASCC3 Arina Puzriakova Phenotypes for gene: ASCC3 were changed from AUTOSOMAL RECESSIVE MENTAL RETARDATION to Intellectual developmental disorder, autosomal recessive 81, OMIM:620700
DDG2P v3.86 ASCC3 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Intellectual developmental disorder, autosomal recessive 81, OMIM:620700)
DDG2P v3.86 ASCC3 Arina Puzriakova Phenotypes for gene: ASCC3 were changed from AUTOSOMAL RECESSIVE MENTAL RETARDATION to Intellectual developmental disorder, autosomal recessive 81, OMIM:620700
Intellectual disability v5.514 ASCC3 Arina Puzriakova Tag gene-checked was removed from gene: ASCC3.
DDG2P v3.85 ASCC3 Arina Puzriakova Tag gene-checked was removed from gene: ASCC3.
Renal ciliopathies v3.5 DLG5 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Yuksel-Vogel-Bauser syndrome, OMIM:620703)
Renal ciliopathies v3.5 DLG5 Arina Puzriakova Phenotypes for gene: DLG5 were changed from DLG5-associated developmental disorder (monoallelic); DLG5-associated developmental disorder (biallelic) to Yuksel-Vogel-Bauser syndrome, OMIM:620703
Unexplained young onset end-stage renal disease v3.40 DLG5 Arina Puzriakova Phenotypes for gene: DLG5 were changed from DLG5-associated developmental disorder (monoallelic); DLG5-associated developmental disorder (biallelic) to Yuksel-Vogel-Bauser syndrome, OMIM:620703
Renal ciliopathies v3.4 DLG5 Arina Puzriakova Tag gene-checked was removed from gene: DLG5.
Intellectual disability v5.514 PTRHD1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities, OMIM:620747)
Intellectual disability v5.514 PTRHD1 Arina Puzriakova Phenotypes for gene: PTRHD1 were changed from Intellectual disability; Parkinsonism to Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities, OMIM:620747
Parkinson Disease and Complex Parkinsonism v1.121 PTRHD1 Arina Puzriakova Phenotypes for gene: PTRHD1 were changed from Intellectual disability; Parkinsonism to Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities, OMIM:620747
Intellectual disability v5.513 PTRHD1 Arina Puzriakova Tag gene-checked was removed from gene: PTRHD1.
DDG2P v3.85 FZD5 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Microphthalmia/coloboma 11, OMIM:620731)
DDG2P v3.85 FZD5 Arina Puzriakova Phenotypes for gene: FZD5 were changed from Autosomal Dominant Coloboma to Microphthalmia/coloboma 11, OMIM:620731
Structural eye disease v3.76 FZD5 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Microphthalmia/coloboma 11, OMIM:620731)
Structural eye disease v3.76 FZD5 Arina Puzriakova Phenotypes for gene: FZD5 were changed from Coloboma, None to Microphthalmia/coloboma 11, OMIM:620731
Fetal anomalies v3.147 FZD5 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Microphthalmia/coloboma 11, OMIM:620731)
Fetal anomalies v3.147 FZD5 Arina Puzriakova Phenotypes for gene: FZD5 were changed from Autosomal Dominant Coloboma to Microphthalmia/coloboma 11, OMIM:620731
Ocular coloboma v1.47 FZD5 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Microphthalmia/coloboma 11, OMIM:620731)
Ocular coloboma v1.47 FZD5 Arina Puzriakova Phenotypes for gene: FZD5 were changed from Coloboma to Microphthalmia/coloboma 11, OMIM:620731
Structural eye disease v3.75 FZD5 Arina Puzriakova Tag gene-checked was removed from gene: FZD5.
DDG2P v3.84 FZD5 Arina Puzriakova Tag gene-checked was removed from gene: FZD5.
Ocular coloboma v1.46 FZD5 Arina Puzriakova Tag gene-checked was removed from gene: FZD5.
Intellectual disability v5.513 SLC32A1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Developmental and epileptic encephalopathy 114, OMIM:620774)
Intellectual disability v5.513 SLC32A1 Arina Puzriakova Phenotypes for gene: SLC32A1 were changed from developmental and epileptic encephalopathy, MONDO:0100062 to Developmental and epileptic encephalopathy 114, OMIM:620774
Early onset or syndromic epilepsy v4.188 SLC32A1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has relevant phenotypes listed in OMIM (Developmental and epileptic encephalopathy 114, OMIM:620774 and Generalized epilepsy with febrile seizures plus, type 12, OMIM:620755)
Early onset or syndromic epilepsy v4.188 SLC32A1 Arina Puzriakova Phenotypes for gene: SLC32A1 were changed from developmental and epileptic encephalopathy, MONDO:0100062; generalized epilepsy with febrile seizures plus, MONDO:0018214 to Developmental and epileptic encephalopathy 114, OMIM:620774; Generalized epilepsy with febrile seizures plus, type 12, OMIM:620755
DDG2P v3.84 SLC32A1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Developmental and epileptic encephalopathy 114, OMIM:620774)
DDG2P v3.84 SLC32A1 Arina Puzriakova Phenotypes for gene: SLC32A1 were changed from SLC32A1-associated developmental and epileptic encephalopathy to Developmental and epileptic encephalopathy 114, OMIM:620774
Intellectual disability v5.512 SLC32A1 Arina Puzriakova Tag gene-checked was removed from gene: SLC32A1.
Early onset or syndromic epilepsy v4.187 SLC32A1 Arina Puzriakova Tag gene-checked was removed from gene: SLC32A1.
DDG2P v3.83 SLC32A1 Arina Puzriakova Tag gene-checked was removed from gene: SLC32A1.
DDG2P v3.83 BRD4 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a phenotype listed in OMIM (Cornelia de Lange syndrome 6, OMIM:620568)
DDG2P v3.83 BRD4 Arina Puzriakova Phenotypes for gene: BRD4 were changed from CORNELIA DE LANGE-LIKE SYNDROME to Cornelia de Lange syndrome 6, OMIM:620568
Severe microcephaly v4.67 BRD4 Arina Puzriakova Phenotypes for gene: BRD4 were changed from Cornelia de Lange-like syndrome, MONDO:0016033 to Cornelia de Lange syndrome 6, OMIM:620568
Intellectual disability v5.512 BRD4 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a phenotype listed in OMIM (Cornelia de Lange syndrome 6, OMIM:620568)
Intellectual disability v5.512 BRD4 Arina Puzriakova Phenotypes for gene: BRD4 were changed from Intellectual disability; Microcephaly; Abnormal heart morphology; Abnormality of the face to Cornelia de Lange syndrome 6, OMIM:620568
DDG2P v3.82 BRD4 Arina Puzriakova Tag gene-checked was removed from gene: BRD4.
Intellectual disability v5.511 BRD4 Arina Puzriakova Tag gene-checked was removed from gene: BRD4.
Intellectual disability v5.511 CAPRIN1 Arina Puzriakova Publications for gene: CAPRIN1 were set to 23849776; 35979925; 36136249
Early onset or syndromic epilepsy v4.187 CAPRIN1 Arina Puzriakova Publications for gene: CAPRIN1 were set to 35979925
DDG2P v3.82 CAPRIN1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a relevant phenotype listed in OMIM (Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636)
DDG2P v3.82 CAPRIN1 Arina Puzriakova Phenotypes for gene: CAPRIN1 were changed from Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636 to Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636
Intellectual disability v5.510 CAPRIN1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a phenotype listed in OMIM (Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636)
Intellectual disability v5.510 CAPRIN1 Arina Puzriakova Phenotypes for gene: CAPRIN1 were changed from Global developmental delay; Delayed speech and language development; Intellectual disability; Autistic behaviour; Seizures to Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636
Early onset or syndromic epilepsy v4.186 CAPRIN1 Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a phenotype listed in OMIM (Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636)
Early onset or syndromic epilepsy v4.186 CAPRIN1 Arina Puzriakova Phenotypes for gene: CAPRIN1 were changed from Global developmental delay; Delayed speech and language development; Intellectual disability; Autistic behavior; Seizures to Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636
Intellectual disability v5.509 CAPRIN1 Arina Puzriakova Tag gene-checked was removed from gene: CAPRIN1.
Early onset or syndromic epilepsy v4.185 CAPRIN1 Arina Puzriakova Tag gene-checked was removed from gene: CAPRIN1.
DDG2P v3.81 CAPRIN1 Arina Puzriakova Phenotypes for gene: CAPRIN1 were changed from AUTISM OR INTELLECTUAL DISABILITY to Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636
DDG2P v3.80 CAPRIN1 Arina Puzriakova Tag gene-checked was removed from gene: CAPRIN1.
Ataxia and cerebellar anomalies - narrow panel v4.59 CAPRIN1 Arina Puzriakova Phenotypes for gene: CAPRIN1 were changed from Cerebellar ataxia, MONDO:0000437; Early-onset ataxia to Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline, OMIM:620636
DDG2P v3.80 WNK3 Arina Puzriakova Tag gene-checked was removed from gene: WNK3.
DDG2P v3.80 WNK3 Arina Puzriakova Phenotypes for gene: WNK3 were changed from WNK3-related neurodevelopmental disorder to WNK3-related neurodevelopmental disorder; Prieto syndrome, OMIM:309610
Autism v0.36 WNK3 Arina Puzriakova Tag gene-checked was removed from gene: WNK3.
Early onset or syndromic epilepsy v4.185 WNK3 Arina Puzriakova Tag gene-checked was removed from gene: WNK3.
Intellectual disability v5.509 WNK3 Arina Puzriakova Phenotypes for gene: WNK3 were changed from X-linked intellectual disability, MONDO:0100284 to Prieto syndrome, OMIM:309610; Intellectual disability, MONDO:0001071
Early onset or syndromic epilepsy v4.185 WNK3 Arina Puzriakova Phenotypes for gene: WNK3 were changed from X-linked intellectual disability, MONDO:0100284 to Prieto syndrome, OMIM:309610; Intellectual disability, MONDO:0001071
Intellectual disability v5.508 WNK3 Arina Puzriakova Tag gene-checked was removed from gene: WNK3.
Malformations of cortical development v4.26 WNK3 Arina Puzriakova Phenotypes for gene: WNK3 were changed from Intellectual disability, MONDO:0001071 to Prieto syndrome, OMIM:309610; Intellectual disability, MONDO:0001071
Malformations of cortical development v4.25 WNK3 Arina Puzriakova Tag gene-checked was removed from gene: WNK3.
Intellectual disability v5.508 C12orf4 Arina Puzriakova Phenotypes for gene: C12orf4 were changed from Autosomal recessive intellectual disability to Intellectual developmental disorder, autosomal recessive 66, OMIM:618221
Severe Paediatric Disorders v1.183 C12orf4 Arina Puzriakova Phenotypes for gene: C12orf4 were changed from Mental retardation, autosomal recessive 66, 618221 to Intellectual developmental disorder, autosomal recessive 66, OMIM:618221
Severe Paediatric Disorders v1.182 C12orf4 Arina Puzriakova commented on gene: C12orf4
Intellectual disability v5.507 C12orf4 Arina Puzriakova commented on gene: C12orf4
Severe Paediatric Disorders v1.182 C12orf4 Arina Puzriakova Tag new-gene-name tag was added to gene: C12orf4.
Intellectual disability v5.507 C12orf4 Arina Puzriakova Tag new-gene-name tag was added to gene: C12orf4.
Mosaic skin disorders - deep sequencing v2.47 MVD Arina Puzriakova Tag Q2_24_promote_green tag was added to gene: MVD.
Mosaic skin disorders - deep sequencing v2.47 MVD Arina Puzriakova Classified gene: MVD as Amber List (moderate evidence)
Mosaic skin disorders - deep sequencing v2.47 MVD Arina Puzriakova Added comment: Comment on list classification: At least 5 individuals reported (PMID: 30942823; 33491095) which meets the criteria for classifying this gene-disease association as Green at the next GMS panel update.
Mosaic skin disorders - deep sequencing v2.47 MVD Arina Puzriakova Gene: mvd has been classified as Amber List (Moderate Evidence).
Mosaic skin disorders - deep sequencing v2.46 MVD Arina Puzriakova commented on gene: MVD
Mosaic skin disorders - deep sequencing v2.46 MVD Arina Puzriakova Publications for gene: MVD were set to 30942823
Mosaic skin disorders - deep sequencing v2.45 MVD Arina Puzriakova Phenotypes for gene: MVD were changed from Linear porokeratosis to Porokeratosis 7, multiple types, OMIM:614714
Rare genetic inflammatory skin disorders v3.7 MVD Arina Puzriakova Phenotypes for gene: MVD were changed from POROKERATOSIS 7, MULTIPLE TYPES, OMIM:614714 to Porokeratosis 7, multiple types, OMIM:614714
Familial disseminated superficial actinic porokeratosis v1.3 MVD Arina Puzriakova Phenotypes for gene: MVD were changed from Porokeratosis 7, multiple types, 614714; actinic/non-actinic disseminated superficial porokeratosis; POROK7; DSAP/DSP to Porokeratosis 7, multiple types, OMIM:614714
Skeletal dysplasia v4.55 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti 308300; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency 300301 to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Primary lymphoedema v3.11 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency 300301 to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Intellectual disability v5.507 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, type II, 308300Ectodermal dysplasia, hypohidrotic, with immune deficiency, 300291Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301Immunodeficiency, isolated, 300584{Atypical mycobacteriosis, familial}, 300636Invasive pneumococcal disease, recurrent isolated, 2, 300640; INCONTINENTIA PIGMENTI (IP) to Incontinentia pigmenti, OMIM:308300
Incontinentia pigmenti v1.2 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from to Incontinentia pigmenti, OMIM:308300
Structural eye disease v3.75 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, IP, 308300 to Incontinentia pigmenti, OMIM:308300
Retinal disorders v4.82 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, 308300 to Incontinentia pigmenti, OMIM:308300
Early onset or syndromic epilepsy v4.184 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, 308300 to Incontinentia pigmenti, OMIM:308300
Mosaic skin disorders - deep sequencing v2.44 IKBKG Arina Puzriakova changed review comment from: Comment on list classification: Incontinentia pigmenti (IP) is a X-linked dominant disorder associated with variants in the IKBKG gene. IP is mostly lethal in males in utero, and only very rare surviving male cases have somatic mosaicism. Phenotypically, cutaneous lesions manifest in Blaschkoid distribution.

Overall 'R327 Mosaic skin disorders - deep sequencing' represents the most likely diagnostic route for these cases and therefore a Green rating on this panel would be appropriate.; to: Comment on list classification: Incontinentia pigmenti (IP) is a X-linked dominant disorder associated with variants in the IKBKG gene. IP is mostly lethal in males in utero, and only very rare surviving male cases have somatic mosaicism. Phenotypically, cutaneous lesions manifest in Blaschkoid distribution.

Overall 'R327 Mosaic skin disorders - deep sequencing' represents a plausible route for referral and diagnosis for these cases and therefore a Green rating on this panel would be appropriate.
Primary immunodeficiency or monogenic inflammatory bowel disease v4.197 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Immunodeficiency 33, 300636; Ectodermal dysplasia, hypohidrotic, with immune deficiency 300291; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301; Immunodeficiency, isolated, 300584; Invasive pneumococcal disease, recurrent isolated, 2,300640; Defects of TLR/NFkappa-B signalling; Anhidrotic ectodermal dysplasia (in some), various infections (bacteria, mycobacteria, viruses and fungi), colitis, conical teeth, variable defects of skin, hair and teeth, monocyte dysfunction; Combined immunodeficiencies with associated or syndromic features to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291; Immunodeficiency 33, OMIM:300636
Rare genetic inflammatory skin disorders v3.6 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti; Incontinentia pigmenti, Ectodermal dysplasia to Incontinentia pigmenti, OMIM:308300
Ectodermal dysplasia without a known gene mutation v1.28 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, type II, 308300; Ectodermal dysplasia, hypohidrotic, with immune deficiency, 300291; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301; Immunodeficiency, isolated, 300584; {Atypical mycobacteriosis, familial}, 300636:Invasive pneumococcal disease, recurrent isolated, 2, 300640; Ectodermal Dysplasia, Hypohidrotic, With Immune Deficiency to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Ectodermal dysplasia v3.29 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Ectodermal Dysplasia, Hypohidrotic, With Immune Deficiency; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301; {Atypical mycobacteriosis, familial}, 300636:Invasive pneumococcal disease, recurrent isolated, 2, 300640; Immunodeficiency, isolated, 300584; Ectodermal dysplasia, hypohidrotic, with immune deficiency, 300291; Incontinentia pigmenti, type II, 308300 to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Gastrointestinal epithelial barrier disorders v1.75 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Immunodeficiency 33, 300636; Immunodeficiency, isolated, 300584 to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Infantile enterocolitis & monogenic inflammatory bowel disease v1.43 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Ectodermal X-linked dysplasia, hypohidrotic, with immune deficiency 300291 to Ectodermal dysplasia and immunodeficiency 1, OMIM:300291
Mosaic skin disorders - deep sequencing v2.44 IKBKG Arina Puzriakova Classified gene: IKBKG as Amber List (moderate evidence)
Mosaic skin disorders - deep sequencing v2.44 IKBKG Arina Puzriakova Added comment: Comment on list classification: Incontinentia pigmenti (IP) is a X-linked dominant disorder associated with variants in the IKBKG gene. IP is mostly lethal in males in utero, and only very rare surviving male cases have somatic mosaicism. Phenotypically, cutaneous lesions manifest in Blaschkoid distribution.

Overall 'R327 Mosaic skin disorders - deep sequencing' represents the most likely diagnostic route for these cases and therefore a Green rating on this panel would be appropriate.
Mosaic skin disorders - deep sequencing v2.44 IKBKG Arina Puzriakova Gene: ikbkg has been classified as Amber List (Moderate Evidence).
Mosaic skin disorders - deep sequencing v2.43 IKBKG Arina Puzriakova Tag somatic tag was added to gene: IKBKG.
Tag Q2_24_promote_green tag was added to gene: IKBKG.
Mosaic skin disorders - deep sequencing v2.43 IKBKG Arina Puzriakova Publications for gene: IKBKG were set to
Mosaic skin disorders - deep sequencing v2.42 IKBKG Arina Puzriakova Phenotypes for gene: IKBKG were changed from Ectodermal dysplasia and immunodeficiency 1, 300291; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301; Incontinentia pigmenti, 308300 to Incontinentia pigmenti, OMIM:308300
Retinal disorders v4.81 SAMD7 Arina Puzriakova commented on gene: SAMD7
Rare genetic inflammatory skin disorders v3.5 ADAMTS2 Dmitrijs Rots reviewed gene: ADAMTS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Thoracic aortic aneurysm or dissection (GMS) v3.8 SECISBP2 krishna chatterjee gene: SECISBP2 was added
gene: SECISBP2 was added to Thoracic aortic aneurysm or dissection (GMS). Sources: Literature
Mode of inheritance for gene: SECISBP2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SECISBP2 were set to PMID 38042913; PMID 21084748
Phenotypes for gene: SECISBP2 were set to Growth retardation; sensorineural hearing loss; muscular dystrophy; thoracic aortic aneurysm; raised circulating thyroxine and low plasma selenium
Penetrance for gene: SECISBP2 were set to Complete
Review for gene: SECISBP2 was set to GREEN
Added comment: Biallelic defects in this gene cause a multi system disorder with deficiency of most human selenoproteins. Phenotypes listed here are associated with a biochemical signature of elevated circulating T4 (thyroxine) and low plasma selenium.

Since some pathogenic variants can be in non-coding regions and cryptic, we suggest a high index of suspicion even in cases of aortic aneurysm with an apparently monoallelic SECISBP2 defect. In such cases, we advocate measuring circulating T4 and selenium; if these biomarker levels are abnormal a cryptic mutation on the other allele should be sought.
Sources: Literature
Childhood onset hereditary spastic paraplegia v4.39 RTN2 Nour Elkhateeb reviewed gene: RTN2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 38527963; Phenotypes: Weakness in the distal upper and lower limbs, Lower limb spasticity, Hyperreflexia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary spastic paraplegia v1.308 RTN2 Nour Elkhateeb changed review comment from: A recent publication has been described seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven consanguineous families with distal hereditary motor neuropathy (dHMN) with pyramidal features.; to: A recent publication has been described seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven consanguineous families with distal hereditary motor neuropathy (dHMN) with pyramidal features.
Hereditary spastic paraplegia v1.308 RTN2 Nour Elkhateeb changed review comment from: A recent publication has described seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven consanguineous families with distal hereditary motor neuropathy (dHMN) with pyramidal features.; to: A recent publication has been described seven novel or ultra-rare homozygous loss-of-function RTN2 variants in 14 individuals from seven consanguineous families with distal hereditary motor neuropathy (dHMN) with pyramidal features.
Hereditary spastic paraplegia v1.308 RTN2 Nour Elkhateeb reviewed gene: RTN2: Rating: ; Mode of pathogenicity: None; Publications: PMID: 38527963; Phenotypes: Weakness in the distal upper and lower limbs, Lower limb spasticity, Hyperreflexia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary ataxia v1.332 FGF14 Evan Reid reviewed gene: FGF14: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMC10844931; Phenotypes: Adult onset cerebellar ataxia, adult onsent episodic ataxia, cerebellar oculomotor disturbances, vestibulopathy, peripheral neuropathy, dysautonomia, spasticity, parkinsonism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Hydrocephalus v4.4 HYLS1 Arina Puzriakova Tag founder-effect tag was added to gene: HYLS1.
Intellectual disability v5.506 ZFX Tracy Lester reviewed gene: ZFX: Rating: GREEN; Mode of pathogenicity: None; Publications: 38325380; Phenotypes: Intellectual disability, developmental delay, behavioural abnormalities, hypotonia, dysmorphic facies; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability v5.506 CLEC16A Arina Puzriakova Tag Q1_24_promote_green tag was added to gene: CLEC16A.
Intellectual disability v5.506 GLI3 Tracy Lester reviewed gene: GLI3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Cystic kidney disease v4.24 CLCN5 John Sayer gene: CLCN5 was added
gene: CLCN5 was added to Cystic kidney disease. Sources: Literature
Mode of inheritance for gene: CLCN5 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: CLCN5 were set to 7922301; 37641036
Phenotypes for gene: CLCN5 were set to cystic kdiney disease; cortical cysts; medullary cysts; nephrocalcinosis; low molecular weight proteinuria; hypercalciuria
Penetrance for gene: CLCN5 were set to Complete
Review for gene: CLCN5 was set to GREEN
Added comment: Oliver Wrong noted kidney cysts in 33% of his cohort and I think Dent disease is such a difficult diagnosis to make, adding it to the cystic panel will identify new cases presenting with mild cystic kidney disease
Sources: Literature
Monogenic short stature v0.168 ISCA-37429-Loss Arina Puzriakova Entity copied from Growth failure in early childhood v3.87
Monogenic short stature v0.168 ISCA-37429-Loss Arina Puzriakova Region: ISCA-37429-Loss was added
Region: ISCA-37429-Loss was added to Monogenic short stature. Sources: Expert Review Red,ClinGen
Mode of inheritance for Region: ISCA-37429-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for Region: ISCA-37429-Loss were set to 20026556; 14630905
Phenotypes for Region: ISCA-37429-Loss were set to Wolf-Hirschhorn syndrome, OMIM:194190
Monogenic short stature v0.167 ISCA-37420-Loss Arina Puzriakova Entity copied from Growth failure in early childhood v3.87
Monogenic short stature v0.167 ISCA-37420-Loss Arina Puzriakova Region: ISCA-37420-Loss was added
Region: ISCA-37420-Loss was added to Monogenic short stature. Sources: Expert Review Red,ClinGen
Mode of inheritance for Region: ISCA-37420-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for Region: ISCA-37420-Loss were set to 25217958; 18628315
Phenotypes for Region: ISCA-37420-Loss were set to Koolen-De Vries syndrome, OMIM:610443; Developmental delay/intellectual disability, hypotonia, distinctive facial features, congenital malformations, and behavioural feature
Monogenic short stature v0.166 ISCA-37406-Loss Arina Puzriakova Entity copied from Growth failure in early childhood v3.87
Monogenic short stature v0.166 ISCA-37406-Loss Arina Puzriakova Region: ISCA-37406-Loss was added
Region: ISCA-37406-Loss was added to Monogenic short stature. Sources: Expert Review Red,ClinGen
Mode of inheritance for Region: ISCA-37406-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for Region: ISCA-37406-Loss were set to 16783566; 10573006
Phenotypes for Region: ISCA-37406-Loss were set to Chromosome 16p13.3 deletion syndrome, OMIM:610543
Monogenic short stature v0.165 ISCA-37397-Loss Arina Puzriakova Entity copied from Growth failure in early childhood v3.86
Monogenic short stature v0.165 ISCA-37397-Loss Arina Puzriakova Region: ISCA-37397-Loss was added
Region: ISCA-37397-Loss was added to Monogenic short stature. Sources: Expert Review Red,ClinGen
Mode of inheritance for Region: ISCA-37397-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for Region: ISCA-37397-Loss were set to 18179902; 23765049; 21671380
Phenotypes for Region: ISCA-37397-Loss were set to Chromosome 22q11.2 deletion syndrome, distal, OMIM:611867
Monogenic short stature v0.164 ISCA-37392-Loss Arina Puzriakova Entity copied from Growth failure in early childhood v3.85
Monogenic short stature v0.164 ISCA-37392-Loss Arina Puzriakova Region: ISCA-37392-Loss was added
Region: ISCA-37392-Loss was added to Monogenic short stature. Sources: Expert Review Red,ClinGen
Mode of inheritance for Region: ISCA-37392-Loss was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for Region: ISCA-37392-Loss were set to 20301427
Phenotypes for Region: ISCA-37392-Loss were set to Williams-Beuren syndrome, OMIM:194050
Monogenic short stature v0.163 ZPR1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.163 ZPR1 Arina Puzriakova gene: ZPR1 was added
gene: ZPR1 was added to Monogenic short stature. Sources: Literature,Expert Review Red
founder-effect tags were added to gene: ZPR1.
Mode of inheritance for gene: ZPR1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZPR1 were set to 29851065
Phenotypes for gene: ZPR1 were set to ?Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies, OMIM:619321
Monogenic short stature v0.162 XRCC4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.162 XRCC4 Arina Puzriakova gene: XRCC4 was added
gene: XRCC4 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: XRCC4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: XRCC4 were set to 25728776
Phenotypes for gene: XRCC4 were set to short stature, microcephaly, hypothyroidism, diabetes mellitus, progressive ataxia, hypergonadotrophic hypogonadism
Monogenic short stature v0.161 WRN Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.161 WRN Arina Puzriakova gene: WRN was added
gene: WRN was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: WRN was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: WRN were set to Werner syndrome
Monogenic short stature v0.160 THRB Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.160 THRB Arina Puzriakova gene: THRB was added
gene: THRB was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: THRB was set to Unknown
Monogenic short stature v0.159 TBCE Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.159 TBCE Arina Puzriakova gene: TBCE was added
gene: TBCE was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: TBCE was set to BIALLELIC, autosomal or pseudoautosomal
Monogenic short stature v0.158 SPRED1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.158 SPRED1 Arina Puzriakova gene: SPRED1 was added
gene: SPRED1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SPRED1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SPRED1 were set to 19443465; 21548021; 21649642; 19366998; 17704776
Phenotypes for gene: SPRED1 were set to Legius Syndrome; Neurofibromatosis-like syndrome
Monogenic short stature v0.157 SOX3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.84
Monogenic short stature v0.157 SOX3 Arina Puzriakova gene: SOX3 was added
gene: SOX3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SOX3 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: SOX3 were set to 15800844
Phenotypes for gene: SOX3 were set to Mental retardation, X-linked, with isolated growth hormone deficiency, OMIM:300123; Intellectual disability, X-linked, with panhypopituitarism, MONDO:0010252; Panhypopituitarism, X-linked, OMIM:312000; Panhypopituitarism, X-linked, MONDO:0010712
Monogenic short stature v0.156 SOX2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.156 SOX2 Arina Puzriakova gene: SOX2 was added
gene: SOX2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SOX2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Monogenic short stature v0.155 SMC3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.155 SMC3 Arina Puzriakova gene: SMC3 was added
gene: SMC3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SMC3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SMC3 were set to Cornelia De Lange
Monogenic short stature v0.154 SMC1A Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.154 SMC1A Arina Puzriakova gene: SMC1A was added
gene: SMC1A was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SMC1A was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes for gene: SMC1A were set to Cornelia de Lange syndrome 2, OMIM:300590; Cornelia de Lange syndrome 2, MONDO:0010370; Developmental and epileptic encephalopathy 85, with or without midline brain defects, OMIM:301044; Developmental and epileptic encephalopathy, 85, with or without midline brain defects, MONDO:0026771
Monogenic short stature v0.153 SMARCAL1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.153 SMARCAL1 Arina Puzriakova gene: SMARCAL1 was added
gene: SMARCAL1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SMARCAL1 was set to Unknown
Monogenic short stature v0.152 SHOX2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.152 SHOX2 Arina Puzriakova gene: SHOX2 was added
gene: SHOX2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: SHOX2 was set to Unknown
Monogenic short stature v0.151 SAMD9 Arina Puzriakova Entity copied from Growth failure in early childhood v3.83
Monogenic short stature v0.151 SAMD9 Arina Puzriakova gene: SAMD9 was added
gene: SAMD9 was added to Monogenic short stature. Sources: Expert Review Red
missense tags were added to gene: SAMD9.
Mode of inheritance for gene: SAMD9 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: SAMD9 were set to 27182967
Phenotypes for gene: SAMD9 were set to MIRAGE syndrome, 617053
Monogenic short stature v0.150 RPS6KA3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.82
Monogenic short stature v0.150 RPS6KA3 Arina Puzriakova gene: RPS6KA3 was added
gene: RPS6KA3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: RPS6KA3 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes for gene: RPS6KA3 were set to Coffin Lowry
Monogenic short stature v0.149 RPL10 Arina Puzriakova Entity copied from Growth failure in early childhood v3.82
Monogenic short stature v0.149 RPL10 Arina Puzriakova gene: RPL10 was added
gene: RPL10 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: RPL10 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: RPL10 were set to 25316788
Phenotypes for gene: RPL10 were set to Mental retardation, X-linked, syndromic, 35
Monogenic short stature v0.148 ROR2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.82
Monogenic short stature v0.148 ROR2 Arina Puzriakova gene: ROR2 was added
gene: ROR2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: ROR2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ROR2 were set to Robinow syndrome, autosomal recessive, OMIM:268310
Monogenic short stature v0.147 RNU4ATAC Arina Puzriakova Entity copied from Growth failure in early childhood v3.82
Monogenic short stature v0.147 RNU4ATAC Arina Puzriakova gene: RNU4ATAC was added
gene: RNU4ATAC was added to Monogenic short stature. Sources: Expert Review Red
locus-type-rna-small-nuclear tags were added to gene: RNU4ATAC.
Mode of inheritance for gene: RNU4ATAC was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RNU4ATAC were set to 21474760
Phenotypes for gene: RNU4ATAC were set to MOPD I
Monogenic short stature v0.146 RBBP8 Arina Puzriakova Entity copied from Growth failure in early childhood v3.82
Monogenic short stature v0.146 RBBP8 Arina Puzriakova gene: RBBP8 was added
gene: RBBP8 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: RBBP8 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RBBP8 were set to 24389050; 21998596
Phenotypes for gene: RBBP8 were set to seckel syndrome but with proportionate head/height impairment, cafe au lair macules
Monogenic short stature v0.145 RAPSN Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.145 RAPSN Arina Puzriakova gene: RAPSN was added
gene: RAPSN was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: RAPSN was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: RAPSN were set to Fetal akinesia deformation sequence 2, OMIM:618388; Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency, OMIM:616326
Monogenic short stature v0.144 RAD21 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.144 RAD21 Arina Puzriakova gene: RAD21 was added
gene: RAD21 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: RAD21 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: RAD21 were set to Cornelia de Lange syndrome 4, OMIM:614701
Monogenic short stature v0.143 PROP1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.143 PROP1 Arina Puzriakova gene: PROP1 was added
gene: PROP1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: PROP1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PROP1 were set to Pituitary hormone deficiency, combined
Monogenic short stature v0.142 PROKR2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.142 PROKR2 Arina Puzriakova gene: PROKR2 was added
gene: PROKR2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: PROKR2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: PROKR2 were set to 22319038
Phenotypes for gene: PROKR2 were set to hypopituitarism, Hypoplastic corpus callosum, normal or small anterior pituitary, Club foot, syrinx spinal cord, microcephaly, epilepsy
Monogenic short stature v0.141 POU1F1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.141 POU1F1 Arina Puzriakova gene: POU1F1 was added
gene: POU1F1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: POU1F1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: POU1F1 were set to Pituitary hormone deficiency, combined or isolated, 1, OMIM:613038; Variable degree of TSH deficiency
Monogenic short stature v0.140 PNPLA6 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.140 PNPLA6 Arina Puzriakova gene: PNPLA6 was added
gene: PNPLA6 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: PNPLA6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PNPLA6 were set to 25480986
Phenotypes for gene: PNPLA6 were set to Oliver-Mcfarlane syndrome, Trichomegaly, GH deficiency, retinal dystrophy, hypogonadotrophic hypogonadism
Monogenic short stature v0.139 PITX2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.139 PITX2 Arina Puzriakova gene: PITX2 was added
gene: PITX2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: PITX2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: PITX2 were set to AXENFELD-RIEGER SYNDROME
Monogenic short stature v0.138 PCNT Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.138 PCNT Arina Puzriakova gene: PCNT was added
gene: PCNT was added to Monogenic short stature. Sources: Expert Review Red,Expert list
Mode of inheritance for gene: PCNT was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PCNT were set to 18157127; 18174396
Phenotypes for gene: PCNT were set to MOPDII; Seckel syndrome, MOPD type II - growth restrction, microcephaly, prominent nose, micrognathia, squeaky voice, insulin resistance, 210720
Monogenic short stature v0.137 PAPPA2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.137 PAPPA2 Arina Puzriakova gene: PAPPA2 was added
gene: PAPPA2 was added to Monogenic short stature. Sources: Expert Review Red,NHS GMS
gene-checked tags were added to gene: PAPPA2.
Mode of inheritance for gene: PAPPA2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PAPPA2 were set to 26902202; 33875846
Phenotypes for gene: PAPPA2 were set to Short stature, Dauber-Argente type, OMIM:619489
Monogenic short stature v0.136 OTX2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.136 OTX2 Arina Puzriakova gene: OTX2 was added
gene: OTX2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: OTX2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: OTX2 were set to 18728160
Phenotypes for gene: OTX2 were set to Microcephaly, bilateral anopthalmia, developmental delay, cleft palate
Monogenic short stature v0.135 ORC6 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.135 ORC6 Arina Puzriakova gene: ORC6 was added
gene: ORC6 was added to Monogenic short stature. Sources: Expert list,Expert Review Red
Mode of inheritance for gene: ORC6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ORC6 were set to 21358632
Phenotypes for gene: ORC6 were set to Meier-Gorlin syndrome 3, OMIM:613803
Monogenic short stature v0.134 ORC4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.134 ORC4 Arina Puzriakova gene: ORC4 was added
gene: ORC4 was added to Monogenic short stature. Sources: Expert Review Red,Expert list
Mode of inheritance for gene: ORC4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ORC4 were set to 21358632
Phenotypes for gene: ORC4 were set to Meier-Gorlin syndrome 2, OMIM:613800
Monogenic short stature v0.133 ORC1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.133 ORC1 Arina Puzriakova gene: ORC1 was added
gene: ORC1 was added to Monogenic short stature. Sources: Expert list,Expert Review Red
Mode of inheritance for gene: ORC1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ORC1 were set to 21358632
Phenotypes for gene: ORC1 were set to Meier-Gorlin syndrome 1, OMIM:224690
Monogenic short stature v0.132 NIPBL Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.132 NIPBL Arina Puzriakova gene: NIPBL was added
gene: NIPBL was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: NIPBL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: NIPBL were set to Cornelia De Lange
Monogenic short stature v0.131 MCM5 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.131 MCM5 Arina Puzriakova gene: MCM5 was added
gene: MCM5 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: MCM5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MCM5 were set to 28198391
Phenotypes for gene: MCM5 were set to ?Meier-Gorlin syndrome 8
Monogenic short stature v0.130 LIG4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.81
Monogenic short stature v0.130 LIG4 Arina Puzriakova gene: LIG4 was added
gene: LIG4 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: LIG4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LIG4 were set to 11779494; 16088910
Phenotypes for gene: LIG4 were set to microcephaly, growth retardation, immunodeficiency, developmental delay
Monogenic short stature v0.129 LIG1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.80
Monogenic short stature v0.129 LIG1 Arina Puzriakova gene: LIG1 was added
gene: LIG1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: LIG1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LIG1 were set to 1581963; 1351188
Phenotypes for gene: LIG1 were set to immunodeficiency, sun sensitivity, growth reatrdation
Monogenic short stature v0.128 LHX4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.128 LHX4 Arina Puzriakova gene: LHX4 was added
gene: LHX4 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: LHX4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: LHX4 were set to 11567216, 18073311
Phenotypes for gene: LHX4 were set to hypopituitarism
Monogenic short stature v0.127 LHX3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.127 LHX3 Arina Puzriakova gene: LHX3 was added
gene: LHX3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: LHX3 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LHX3 were set to GH, TSH, LH, FSH, PRL deficiencies
Monogenic short stature v0.126 KMT2D Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.126 KMT2D Arina Puzriakova gene: KMT2D was added
gene: KMT2D was added to Monogenic short stature. Sources: Expert Review Red,NHS GMS
Mode of inheritance for gene: KMT2D was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KMT2D were set to 31949313; 32083401; 21882399
Phenotypes for gene: KMT2D were set to Kabuki syndrome 1, OMIM:147920
Monogenic short stature v0.125 KHDC3L Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.125 KHDC3L Arina Puzriakova gene: KHDC3L was added
gene: KHDC3L was added to Monogenic short stature. Sources: Expert list,Expert Review Red
watchlist tags were added to gene: KHDC3L.
Mode of inheritance for gene: KHDC3L was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: KHDC3L were set to 29574422
Phenotypes for gene: KHDC3L were set to IUGR; Failure to thrive; Hydatidiform mole, recurrent, 2 OMIM:614293; hydatidiform mole, recurrent, 2 MONDO:0013671; pregnancy loss
Penetrance for gene: KHDC3L were set to unknown
Monogenic short stature v0.124 KDM6A Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.124 KDM6A Arina Puzriakova gene: KDM6A was added
gene: KDM6A was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: KDM6A was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: KDM6A were set to 23913813; 29914387; 31654559; 33674768
Phenotypes for gene: KDM6A were set to Kabuki syndrome 2, OMIM:300867
Monogenic short stature v0.123 INTS8 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.123 INTS8 Arina Puzriakova gene: INTS8 was added
gene: INTS8 was added to Monogenic short stature. Sources: Literature
Mode of inheritance for gene: INTS8 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: INTS8 were set to 28542170
Phenotypes for gene: INTS8 were set to ?Neurodevelopmental disorder with cerebellar hypoplasia and spasticity, OMIM:618572
Monogenic short stature v0.122 INSR Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.122 INSR Arina Puzriakova gene: INSR was added
gene: INSR was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: INSR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: INSR were set to Leprechaunism
Monogenic short stature v0.121 IGFBP3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.121 IGFBP3 Arina Puzriakova gene: IGFBP3 was added
gene: IGFBP3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: IGFBP3 was set to Unknown
Publications for gene: IGFBP3 were set to 10364674
Phenotypes for gene: IGFBP3 were set to Silver Russell Syndrome
Monogenic short stature v0.120 IGFBP1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.120 IGFBP1 Arina Puzriakova gene: IGFBP1 was added
gene: IGFBP1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: IGFBP1 was set to Unknown
Publications for gene: IGFBP1 were set to 10364674
Phenotypes for gene: IGFBP1 were set to Silver-Russell Syndrome
Monogenic short stature v0.119 IFT172 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.119 IFT172 Arina Puzriakova gene: IFT172 was added
gene: IFT172 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: IFT172 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IFT172 were set to 25664603
Phenotypes for gene: IFT172 were set to GH deficiency, retinopathy, metaphyseal dysplasia
Monogenic short stature v0.118 HESX1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.118 HESX1 Arina Puzriakova gene: HESX1 was added
gene: HESX1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: HESX1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: HESX1 were set to Growth hormone deficiency with pituitary anomalies, OMIM:182230; Pituitary hormone deficiency, combined, 5, OMIM:182230; Septooptic dysplasia, OMIM:182230
Monogenic short stature v0.117 HDAC8 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.117 HDAC8 Arina Puzriakova gene: HDAC8 was added
gene: HDAC8 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: HDAC8 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes for gene: HDAC8 were set to Cornelia De Lange
Monogenic short stature v0.116 H19 Arina Puzriakova Entity copied from Growth failure in early childhood v3.79
Monogenic short stature v0.116 H19 Arina Puzriakova gene: H19 was added
gene: H19 was added to Monogenic short stature. Sources: Expert Review Red
locus-type-rna-long-non-coding tags were added to gene: H19.
Mode of inheritance for gene: H19 was set to Other
Phenotypes for gene: H19 were set to Russell-Silver syndrome
Monogenic short stature v0.115 GPR161 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.115 GPR161 Arina Puzriakova gene: GPR161 was added
gene: GPR161 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GPR161 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GPR161 were set to 25322266
Phenotypes for gene: GPR161 were set to Short stature with hypopituitarism, intellectual disability, sparse or absent hair in the frontal area, hypotelorism, broad nasal root, thick alae nasi, nail hypoplasia, short fifth finger, 2-3 toe syndactyl. MRI showed hypoplastic pituitary gland, empty sella, ectopic neurohypophysis, and interrupted pituitary stalk
Monogenic short stature v0.114 GLI3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.114 GLI3 Arina Puzriakova gene: GLI3 was added
gene: GLI3 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GLI3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GLI3 were set to 9054938
Phenotypes for gene: GLI3 were set to Pallister-Hall syndrome
Monogenic short stature v0.113 GLI2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.113 GLI2 Arina Puzriakova gene: GLI2 was added
gene: GLI2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GLI2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: GLI2 were set to Holoprosencephaly, hypopituitarism
Monogenic short stature v0.112 GINS3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.112 GINS3 Arina Puzriakova gene: GINS3 was added
gene: GINS3 was added to Monogenic short stature. Sources: Expert Review Red,Literature
gene-checked tags were added to gene: GINS3.
Mode of inheritance for gene: GINS3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GINS3 were set to 35603789
Phenotypes for gene: GINS3 were set to Meier-Gorlin syndrome like; Meier-Gorlin syndrome, MONDO:0016817
Penetrance for gene: GINS3 were set to unknown
Mode of pathogenicity for gene: GINS3 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.111 GINS2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.111 GINS2 Arina Puzriakova gene: GINS2 was added
gene: GINS2 was added to Monogenic short stature. Sources: Literature,Expert Review Red
Mode of inheritance for gene: GINS2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GINS2 were set to 34353863
Phenotypes for gene: GINS2 were set to Meier-Gorlin syndrome like; Meier-Gorlin syndrome, MONDO:0016817
Penetrance for gene: GINS2 were set to unknown
Mode of pathogenicity for gene: GINS2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.110 GHSR Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.110 GHSR Arina Puzriakova gene: GHSR was added
gene: GHSR was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GHSR was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: GHSR were set to 16511605
Phenotypes for gene: GHSR were set to Idiopathic short stature, GH deficiency
Monogenic short stature v0.109 GHRHR Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.109 GHRHR Arina Puzriakova gene: GHRHR was added
gene: GHRHR was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GHRHR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GHRHR were set to Growth hormone deficiency
Monogenic short stature v0.108 GH1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.108 GH1 Arina Puzriakova gene: GH1 was added
gene: GH1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: GH1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: GH1 were set to Growth hormone deficiency
Monogenic short stature v0.107 FGFR1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.107 FGFR1 Arina Puzriakova gene: FGFR1 was added
gene: FGFR1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: FGFR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: FGFR1 were set to 22319038
Monogenic short stature v0.106 FGF8 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.106 FGF8 Arina Puzriakova gene: FGF8 was added
gene: FGF8 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: FGF8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: FGF8 were set to 22319038
Phenotypes for gene: FGF8 were set to hypopituitarism, absent corpus callosum, Holoprosencephaly, Moebius syndrome, craniofacial defects, high arched palate, maxillary hypoplasia, microcepahly, spastic diplegia
Monogenic short stature v0.105 FGD1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.105 FGD1 Arina Puzriakova gene: FGD1 was added
gene: FGD1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: FGD1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: FGD1 were set to Aarskog
Monogenic short stature v0.104 FANCM Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.104 FANCM Arina Puzriakova gene: FANCM was added
gene: FANCM was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: FANCM was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FANCM were set to 16116422; 19423727; 25078778
Phenotypes for gene: FANCM were set to Fanconi anemia, complementation group M, 614087
Monogenic short stature v0.103 ERCC8 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.103 ERCC8 Arina Puzriakova gene: ERCC8 was added
gene: ERCC8 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: ERCC8 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ERCC8 were set to cockayne
Monogenic short stature v0.102 ERCC6 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.102 ERCC6 Arina Puzriakova gene: ERCC6 was added
gene: ERCC6 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: ERCC6 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ERCC6 were set to Cockayne syndrome, type B, 133540
Monogenic short stature v0.101 EPHX1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.101 EPHX1 Arina Puzriakova gene: EPHX1 was added
gene: EPHX1 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: EPHX1 was set to Unknown
Phenotypes for gene: EPHX1 were set to ?Fetal hydantoin syndromeDiphenylhydantoin toxicityHypercholanemia, familial, 607748{Preeclampsia, susceptibility to}, 189800
Monogenic short stature v0.100 EP300 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.100 EP300 Arina Puzriakova gene: EP300 was added
gene: EP300 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: EP300 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: EP300 were set to Rubenstein Taybi
Monogenic short stature v0.99 DOK7 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.99 DOK7 Arina Puzriakova gene: DOK7 was added
gene: DOK7 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: DOK7 was set to Unknown
Phenotypes for gene: DOK7 were set to Myasthenia, limb-girdle, familial, 254300Fetal akinesia deformation sequence, 208150
Monogenic short stature v0.98 DNA2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.98 DNA2 Arina Puzriakova gene: DNA2 was added
gene: DNA2 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: DNA2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DNA2 were set to 24389050; 31045292
Phenotypes for gene: DNA2 were set to Seckel syndrome 8, OMIM:615807
Monogenic short stature v0.97 DHCR7 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.97 DHCR7 Arina Puzriakova gene: DHCR7 was added
gene: DHCR7 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: DHCR7 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: DHCR7 were set to Smith Lemli Opitz
Monogenic short stature v0.96 CRIPT Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.96 CRIPT Arina Puzriakova gene: CRIPT was added
gene: CRIPT was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: CRIPT was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CRIPT were set to PMC3912419
Phenotypes for gene: CRIPT were set to frontal bossing, high forehead, sparse hair and eyebrows, telecanthus, mild proptosis (staring look), upturned nostrils, and hypoplastic terminal phalanges with brachydactyly
Monogenic short stature v0.95 CREBBP Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.95 CREBBP Arina Puzriakova gene: CREBBP was added
gene: CREBBP was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: CREBBP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: CREBBP were set to Rubenstein Taybi
Monogenic short stature v0.94 COL1A1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.94 COL1A1 Arina Puzriakova gene: COL1A1 was added
gene: COL1A1 was added to Monogenic short stature. Sources: Expert list
Mode of inheritance for gene: COL1A1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: COL1A1 were set to OI; Osteogenesis imperfecta, type II, 166210; Osteogenesis imperfecta, type III, 259420; Osteogenesis imperfecta, type I, 166200; Osteogenesis imperfecta, type IV, 166220
Monogenic short stature v0.93 CHD7 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.93 CHD7 Arina Puzriakova gene: CHD7 was added
gene: CHD7 was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: CHD7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CHD7 were set to 16400610
Phenotypes for gene: CHD7 were set to CHARGE syndrome - ocular coloboma, choanal atresia, cranial nerve defects, distinctive external and inner ear abnormalities, hearing loss, cardiovascular malformations, urogenital anomalies, and growth retardation; CHARGE syndrome, 214800
Monogenic short stature v0.92 CENPJ Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.92 CENPJ Arina Puzriakova gene: CENPJ was added
gene: CENPJ was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: CENPJ was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CENPJ were set to 20522431
Phenotypes for gene: CENPJ were set to seckel syndrome
Monogenic short stature v0.91 CDT1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.91 CDT1 Arina Puzriakova gene: CDT1 was added
gene: CDT1 was added to Monogenic short stature. Sources: Expert list,Expert Review Red
Mode of inheritance for gene: CDT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CDT1 were set to 21358632
Phenotypes for gene: CDT1 were set to Meier-Gorlin syndrome 4, OMIM:613804
Monogenic short stature v0.90 CDC6 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.90 CDC6 Arina Puzriakova gene: CDC6 was added
gene: CDC6 was added to Monogenic short stature. Sources: Expert Review Red,Expert list
Mode of inheritance for gene: CDC6 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CDC6 were set to 21358632
Phenotypes for gene: CDC6 were set to ?Meier-Gorlin syndrome 5, 613805; patellar hypoplasia/aplasia, microtia, meier-gorlin syndrome, mammary hypoplasia
Monogenic short stature v0.89 ATRX Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.89 ATRX Arina Puzriakova gene: ATRX was added
gene: ATRX was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: ATRX was set to Unknown
Phenotypes for gene: ATRX were set to SGA, which is sometimes called intrauterine growth restriction (IUGR),
Monogenic short stature v0.88 ATRIP Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.88 ATRIP Arina Puzriakova gene: ATRIP was added
gene: ATRIP was added to Monogenic short stature. Sources: Expert Review Red
Mode of inheritance for gene: ATRIP was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ATRIP were set to 23144622
Phenotypes for gene: ATRIP were set to microcephaly, micrognathia, small ear lobes, dental crowding
Monogenic short stature v0.87 A2ML1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.87 A2ML1 Arina Puzriakova gene: A2ML1 was added
gene: A2ML1 was added to Monogenic short stature. Sources: Expert list,Expert Review Red,NHS GMS
Mode of inheritance for gene: A2ML1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: A2ML1 were set to 24939586; 25862627
Phenotypes for gene: A2ML1 were set to Noonan syndrome
Monogenic short stature v0.86 ZNF668 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.86 ZNF668 Arina Puzriakova gene: ZNF668 was added
gene: ZNF668 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: ZNF668.
Mode of inheritance for gene: ZNF668 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZNF668 were set to 34313816; 26633546
Phenotypes for gene: ZNF668 were set to Neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies, OMIM:620194
Monogenic short stature v0.85 VPS50 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.85 VPS50 Arina Puzriakova gene: VPS50 was added
gene: VPS50 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: VPS50.
Mode of inheritance for gene: VPS50 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: VPS50 were set to 34037727
Phenotypes for gene: VPS50 were set to Neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis, OMIM:619685
Penetrance for gene: VPS50 were set to Complete
Monogenic short stature v0.84 SETD5 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.84 SETD5 Arina Puzriakova gene: SETD5 was added
gene: SETD5 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
Mode of inheritance for gene: SETD5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SETD5 were set to 28881385
Phenotypes for gene: SETD5 were set to Intellectual developmental disorder, autosomal dominant 23, OMIM:615761
Penetrance for gene: SETD5 were set to Incomplete
Monogenic short stature v0.83 RECQL4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.83 RECQL4 Arina Puzriakova gene: RECQL4 was added
gene: RECQL4 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
Q1_24_promote_green, Q1_24_NHS_review tags were added to gene: RECQL4.
Mode of inheritance for gene: RECQL4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RECQL4 were set to 25966250; 29462647; 31406625; 34155702; 35086131; 35781852; 37228773; 38021400
Phenotypes for gene: RECQL4 were set to Rothmund-Thomson syndrome, type 2, OMIM:268400
Penetrance for gene: RECQL4 were set to Complete
Monogenic short stature v0.82 RASA2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.82 RASA2 Arina Puzriakova gene: RASA2 was added
gene: RASA2 was added to Monogenic short stature. Sources: NHS GMS,Expert list,Expert Review Amber
Mode of inheritance for gene: RASA2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: RASA2 were set to 25049390
Phenotypes for gene: RASA2 were set to Noonan syndrome
Monogenic short stature v0.81 RAP1B Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.81 RAP1B Arina Puzriakova gene: RAP1B was added
gene: RAP1B was added to Monogenic short stature. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: RAP1B.
Mode of inheritance for gene: RAP1B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: RAP1B were set to 32627184; 26280580
Phenotypes for gene: RAP1B were set to Syndromic intellectual disability; short stature
Monogenic short stature v0.80 RAD51 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.80 RAD51 Arina Puzriakova gene: RAD51 was added
gene: RAD51 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
Mode of inheritance for gene: RAD51 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: RAD51 were set to 26681308; 26253028; 30907510
Phenotypes for gene: RAD51 were set to Fanconi anemia, complementation group R, OMIM:617244
Monogenic short stature v0.79 PADI6 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.79 PADI6 Arina Puzriakova gene: PADI6 was added
gene: PADI6 was added to Monogenic short stature. Sources: Expert Review Amber,Expert Review
Mode of inheritance for gene: PADI6 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: PADI6 were set to 32928291; 29574422; 33221824
Phenotypes for gene: PADI6 were set to Short stature; IUGR; miscarriages in the family; Preimplantation embryonic lethality 2 OMIM:617234; preimplantation embryonic lethality 2 MONDO:0014978; Beckwith-Wiedemann syndrome; Multi Locus Imprinting Disturbance
Penetrance for gene: PADI6 were set to unknown
Monogenic short stature v0.78 NLRP7 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.78 NLRP7 Arina Puzriakova gene: NLRP7 was added
gene: NLRP7 was added to Monogenic short stature. Sources: Expert list,Expert Review Amber
Mode of inheritance for gene: NLRP7 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: NLRP7 were set to 28561018
Phenotypes for gene: NLRP7 were set to IUGR; Short stature; fetal wastage; Multi Locus Imprinting Disturbance; Hydatidiform mole, recurrent, 1 OMIM:231090; hydatidiform mole, recurrent, 1 MONDO:0009273
Penetrance for gene: NLRP7 were set to unknown
Monogenic short stature v0.77 NLRP5 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.77 NLRP5 Arina Puzriakova gene: NLRP5 was added
gene: NLRP5 was added to Monogenic short stature. Sources: Expert list,Expert Review Amber
Mode of inheritance for gene: NLRP5 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: NLRP5 were set to 26323243; 29574422
Phenotypes for gene: NLRP5 were set to IUGR; Short stature; Failure to thrive; body asymmetry; multilocus imprinting disturbances
Penetrance for gene: NLRP5 were set to unknown
Monogenic short stature v0.76 NLRP2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.76 NLRP2 Arina Puzriakova gene: NLRP2 was added
gene: NLRP2 was added to Monogenic short stature. Sources: Expert list,Expert Review Amber
watchlist tags were added to gene: NLRP2.
Mode of inheritance for gene: NLRP2 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: NLRP2 were set to 26323243; 29574422; 19300480; 30877238; 33090377
Phenotypes for gene: NLRP2 were set to Maternal effect gene- causing phenotypes that include IUGR
Penetrance for gene: NLRP2 were set to unknown
Monogenic short stature v0.75 NF1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.75 NF1 Arina Puzriakova gene: NF1 was added
gene: NF1 was added to Monogenic short stature. Sources: Expert list,Expert Review Amber
Mode of inheritance for gene: NF1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: NF1 were set to 26178382; 27247625; 30602027; 35633639; 36373817
Phenotypes for gene: NF1 were set to Neurofibromatosis-Noonan syndrome, OMIM:601321
Monogenic short stature v0.74 MRAS Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.74 MRAS Arina Puzriakova gene: MRAS was added
gene: MRAS was added to Monogenic short stature. Sources: Expert Review Amber,Expert Review
Mode of inheritance for gene: MRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MRAS were set to 28289718; 31173466; 31108500; 34080768
Phenotypes for gene: MRAS were set to Noonan syndrome 11, OMIM:618499
Monogenic short stature v0.73 MAPK1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.73 MAPK1 Arina Puzriakova gene: MAPK1 was added
gene: MAPK1 was added to Monogenic short stature. Sources: Expert Review Amber,Expert Review
Mode of inheritance for gene: MAPK1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MAPK1 were set to 32721402
Phenotypes for gene: MAPK1 were set to Noonan syndrome 13, OMIM:619087
Mode of pathogenicity for gene: MAPK1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.72 KDM3B Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.72 KDM3B Arina Puzriakova gene: KDM3B was added
gene: KDM3B was added to Monogenic short stature. Sources: Victorian Clinical Genetics Services,Expert Review Amber
watchlist tags were added to gene: KDM3B.
Mode of inheritance for gene: KDM3B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: KDM3B were set to 30929739
Phenotypes for gene: KDM3B were set to Diets-Jongmans syndrome, OMIM:618846; Diets-Jongmans syndrome, MONDO:0030012
Monogenic short stature v0.71 GGPS1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.71 GGPS1 Arina Puzriakova gene: GGPS1 was added
gene: GGPS1 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
Mode of inheritance for gene: GGPS1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GGPS1 were set to 32403198
Phenotypes for gene: GGPS1 were set to Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, OMIM:619518
Monogenic short stature v0.70 FOXP4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.70 FOXP4 Arina Puzriakova gene: FOXP4 was added
gene: FOXP4 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
gene-checked tags were added to gene: FOXP4.
Mode of inheritance for gene: FOXP4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: FOXP4 were set to 33110267
Phenotypes for gene: FOXP4 were set to Neurodevelopmental disorder; multiple congenital abnormalities
Monogenic short stature v0.69 CCDC186 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.69 CCDC186 Arina Puzriakova gene: CCDC186 was added
gene: CCDC186 was added to Monogenic short stature. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: CCDC186.
Mode of inheritance for gene: CCDC186 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CCDC186 were set to 33259146; 28600779
Phenotypes for gene: CCDC186 were set to failure to thrive and developmental delay
Monogenic short stature v0.68 BTK Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.68 BTK Arina Puzriakova gene: BTK was added
gene: BTK was added to Monogenic short stature. Sources: Expert Review Amber
Mode of inheritance for gene: BTK was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: BTK were set to 8013627; 7849697; 9554752
Phenotypes for gene: BTK were set to Isolated growth hormone deficiency, type III, with agammaglobulinaemia, OMIM:307200
Monogenic short stature v0.67 ZFP57 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.67 ZFP57 Arina Puzriakova gene: ZFP57 was added
gene: ZFP57 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: ZFP57 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZFP57 were set to 18622393
Phenotypes for gene: ZFP57 were set to Diabetes mellitus, transient neonatal 1, OMIM:601410
Monogenic short stature v0.66 UBE2T Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.66 UBE2T Arina Puzriakova gene: UBE2T was added
gene: UBE2T was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: UBE2T was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: UBE2T were set to 26046368
Phenotypes for gene: UBE2T were set to Fanconi anemia, complementation group T, OMIM:616435
Monogenic short stature v0.65 TRIM37 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.65 TRIM37 Arina Puzriakova gene: TRIM37 was added
gene: TRIM37 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: TRIM37 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TRIM37 were set to Mulibrey nanism, OMIM:253250
Monogenic short stature v0.64 TOP3A Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.64 TOP3A Arina Puzriakova gene: TOP3A was added
gene: TOP3A was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: TOP3A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TOP3A were set to Microcephaly, growth restriction, and increased sister chromatid exchange 2, OMIM:618097
Monogenic short stature v0.63 STAT5B Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.63 STAT5B Arina Puzriakova gene: STAT5B was added
gene: STAT5B was added to Monogenic short stature. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: STAT5B was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: STAT5B were set to 16787985; 15827093; 17030597; 26703237; 29844444
Phenotypes for gene: STAT5B were set to Growth hormone insensitivity with immune dysregulation 1, autosomal recessive, OMIM:245590; Growth hormone insensitivity with immune dysregulation 2, autosomal dominant, OMIM:618985
Monogenic short stature v0.62 SRCAP Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.62 SRCAP Arina Puzriakova gene: SRCAP was added
gene: SRCAP was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: SRCAP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SRCAP were set to Floating-Harbor syndrome, OMIM:136140
Monogenic short stature v0.61 SPRED2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.61 SPRED2 Arina Puzriakova gene: SPRED2 was added
gene: SPRED2 was added to Monogenic short stature. Sources: Expert Review Green,Literature,NHS GMS
Mode of inheritance for gene: SPRED2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SPRED2 were set to 34626534
Phenotypes for gene: SPRED2 were set to Noonan syndrome 14, OMIM:619745
Monogenic short stature v0.60 SOS2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.78
Monogenic short stature v0.60 SOS2 Arina Puzriakova gene: SOS2 was added
gene: SOS2 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: SOS2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: SOS2 were set to 26173643; 25795793
Phenotypes for gene: SOS2 were set to Noonan syndrome 9, OMIM:616559
Monogenic short stature v0.59 SOS1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.59 SOS1 Arina Puzriakova gene: SOS1 was added
gene: SOS1 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: SOS1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SOS1 were set to 17143285; 17143282; 17586837; 19438935
Phenotypes for gene: SOS1 were set to Noonan syndrome 4, OMIM:610733
Mode of pathogenicity for gene: SOS1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.58 SLX4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.58 SLX4 Arina Puzriakova gene: SLX4 was added
gene: SLX4 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: SLX4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLX4 were set to 21240277; 21240275
Phenotypes for gene: SLX4 were set to Fanconi anemia, complementation group P, OMIM:613951
Monogenic short stature v0.57 SHOX Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.57 SHOX Arina Puzriakova gene: SHOX was added
gene: SHOX was added to Monogenic short stature. Sources: Expert Review Green,NHS GMS
Pseudoautosomal region 1 tags were added to gene: SHOX.
Mode of inheritance for gene: SHOX was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes for gene: SHOX were set to Langer mesomelic dysplasia, OMIM:249700 (PR); Leri-Weill dyschondrosteosis, OMIM:127300 (PD); Short stature, idiopathic familial, OMIM:300582
Monogenic short stature v0.56 SHOC2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.56 SHOC2 Arina Puzriakova gene: SHOC2 was added
gene: SHOC2 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: SHOC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SHOC2 were set to 19684605; 22528146; 23918763
Phenotypes for gene: SHOC2 were set to Noonan syndrome-like with loose anagen hair 1, OMIM:607721
Mode of pathogenicity for gene: SHOC2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.55 RRAS2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.55 RRAS2 Arina Puzriakova gene: RRAS2 was added
gene: RRAS2 was added to Monogenic short stature. Sources: Expert Review Green,Expert Review,NHS GMS
Mode of inheritance for gene: RRAS2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RRAS2 were set to 31130282
Phenotypes for gene: RRAS2 were set to Noonan syndrome 12, OMIM:618624
Mode of pathogenicity for gene: RRAS2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.54 RNPC3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.54 RNPC3 Arina Puzriakova gene: RNPC3 was added
gene: RNPC3 was added to Monogenic short stature. Sources: Expert Review Green,NHS GMS
gene-checked tags were added to gene: RNPC3.
Mode of inheritance for gene: RNPC3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RNPC3 were set to 24480542; 29866761; 32462814; 33650182
Phenotypes for gene: RNPC3 were set to Pituitary hormone deficiency, combined or isolated, 7, OMIM:618160
Monogenic short stature v0.53 RIT1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.53 RIT1 Arina Puzriakova gene: RIT1 was added
gene: RIT1 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: RIT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RIT1 were set to 23791108; 25124994; 24939608
Phenotypes for gene: RIT1 were set to Noonan syndrome 8, OMIM:615355
Mode of pathogenicity for gene: RIT1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.52 RAF1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.52 RAF1 Arina Puzriakova gene: RAF1 was added
gene: RAF1 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: RAF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RAF1 were set to 17603483; 17603482
Phenotypes for gene: RAF1 were set to LEOPARD syndrome 2, OMIM:611554; Noonan syndrome 5, OMIM:611553
Mode of pathogenicity for gene: RAF1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.51 PTPN11 Arina Puzriakova Entity copied from Growth failure in early childhood v3.77
Monogenic short stature v0.51 PTPN11 Arina Puzriakova gene: PTPN11 was added
gene: PTPN11 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: PTPN11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: PTPN11 were set to 17603483; 11704759; 12529711; 12634870; 15384080; 15240615; 16263833; 17497712; 18678287
Phenotypes for gene: PTPN11 were set to LEOPARD syndrome 1, OMIM:151100; Noonan syndrome 1, OMIM:163950
Monogenic short stature v0.50 PPP1CB Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.50 PPP1CB Arina Puzriakova gene: PPP1CB was added
gene: PPP1CB was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: PPP1CB was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: PPP1CB were set to 27264673; 27681385; 28211982
Phenotypes for gene: PPP1CB were set to Noonan syndrome-like disorder with loose anagen hair 2, OMIM:617506
Monogenic short stature v0.49 PLK4 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.49 PLK4 Arina Puzriakova gene: PLK4 was added
gene: PLK4 was added to Monogenic short stature. Sources: Expert Review Green,Literature
Mode of inheritance for gene: PLK4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLK4 were set to 25344692; 25320347; 27650967
Phenotypes for gene: PLK4 were set to Microcephaly and chorioretinopathy, autosomal recessive, 2, OMIM:616171
Monogenic short stature v0.48 PLAG1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.48 PLAG1 Arina Puzriakova gene: PLAG1 was added
gene: PLAG1 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: PLAG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: PLAG1 were set to 28796236
Phenotypes for gene: PLAG1 were set to Silver-Russell syndrome 4, OMIM:618907
Monogenic short stature v0.47 PIK3R1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.47 PIK3R1 Arina Puzriakova gene: PIK3R1 was added
gene: PIK3R1 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: PIK3R1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: PIK3R1 were set to SHORT syndrome, OMIM:269880
Monogenic short stature v0.46 PALB2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.46 PALB2 Arina Puzriakova gene: PALB2 was added
gene: PALB2 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: PALB2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PALB2 were set to 17200672; 17200671
Phenotypes for gene: PALB2 were set to Fanconi anemia, complementation group N, OMIM:610832
Monogenic short stature v0.45 OBSL1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.45 OBSL1 Arina Puzriakova gene: OBSL1 was added
gene: OBSL1 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: OBSL1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: OBSL1 were set to 21737058
Phenotypes for gene: OBSL1 were set to 3-M syndrome 2, OMIM:612921
Monogenic short stature v0.44 NRAS Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.44 NRAS Arina Puzriakova gene: NRAS was added
gene: NRAS was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: NRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NRAS were set to 19966803; 19775298
Phenotypes for gene: NRAS were set to Noonan syndrome 6, OMIM:613224
Mode of pathogenicity for gene: NRAS was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.43 NPR2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.43 NPR2 Arina Puzriakova gene: NPR2 was added
gene: NPR2 was added to Monogenic short stature. Sources: NHS GMS,Expert list,Expert Review Green
Mode of inheritance for gene: NPR2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: NPR2 were set to Acromesomelic dysplasia 1, Maroteaux type, OMIM:602875
Monogenic short stature v0.42 NHLRC2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.42 NHLRC2 Arina Puzriakova gene: NHLRC2 was added
gene: NHLRC2 was added to Monogenic short stature. Sources: Expert Review Green,Literature
gene-checked tags were added to gene: NHLRC2.
Mode of inheritance for gene: NHLRC2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NHLRC2 were set to 29423877; 32435055
Phenotypes for gene: NHLRC2 were set to FINCA syndrome, OMIM:618278
Monogenic short stature v0.41 NBN Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.41 NBN Arina Puzriakova gene: NBN was added
gene: NBN was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: NBN was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: NBN were set to Nijmegen breakage syndrome, OMIM:251260
Monogenic short stature v0.40 NBAS Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.40 NBAS Arina Puzriakova gene: NBAS was added
gene: NBAS was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: NBAS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NBAS were set to 31761904
Phenotypes for gene: NBAS were set to Short stature, optic nerve atrophy, and Pelger-Huet anomaly, OMIM:614800
Monogenic short stature v0.39 MTX2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.39 MTX2 Arina Puzriakova gene: MTX2 was added
gene: MTX2 was added to Monogenic short stature. Sources: Expert Review Green,Expert Review,Literature
Mode of inheritance for gene: MTX2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MTX2 were set to 32917887
Phenotypes for gene: MTX2 were set to Mandibuloacral dysplasia progeroid syndrome, OMIM:619127
Monogenic short stature v0.38 MSTO1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.38 MSTO1 Arina Puzriakova gene: MSTO1 was added
gene: MSTO1 was added to Monogenic short stature. Sources: Expert Review Green,Literature,NHS GMS
Q1_24_MOI, Q1_24_NHS_review tags were added to gene: MSTO1.
Mode of inheritance for gene: MSTO1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: MSTO1 were set to 29339779; 28544275; 31604776; 31130378; 28554942; 37431817
Phenotypes for gene: MSTO1 were set to Myopathy, mitochondrial, and ataxia, OMIM:617675
Monogenic short stature v0.37 MAP2K2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.37 MAP2K2 Arina Puzriakova gene: MAP2K2 was added
gene: MAP2K2 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: MAP2K2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MAP2K2 were set to 16439621; 21396583; 23379592
Phenotypes for gene: MAP2K2 were set to Cardiofaciocutaneous syndrome 4, OMIM:615280
Mode of pathogenicity for gene: MAP2K2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.36 MAP2K1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.36 MAP2K1 Arina Puzriakova gene: MAP2K1 was added
gene: MAP2K1 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: MAP2K1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MAP2K1 were set to 16825433; 16439621; 21396583; 23321623
Phenotypes for gene: MAP2K1 were set to Cardiofaciocutaneous syndrome 3, OMIM:615279
Mode of pathogenicity for gene: MAP2K1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.35 LZTR1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.35 LZTR1 Arina Puzriakova gene: LZTR1 was added
gene: LZTR1 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: LZTR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: LZTR1 were set to 29469822; 25795793
Phenotypes for gene: LZTR1 were set to Noonan syndrome 10, OMIM:616564 (AD); Noonan syndrome 2, OMIM:605275 (AR)
Monogenic short stature v0.34 KRAS Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.34 KRAS Arina Puzriakova gene: KRAS was added
gene: KRAS was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: KRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KRAS were set to 21396583
Phenotypes for gene: KRAS were set to Cardiofaciocutaneous syndrome 2, OMIM:615278; Noonan syndrome 3, OMIM:609942
Mode of pathogenicity for gene: KRAS was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.33 INTS1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.33 INTS1 Arina Puzriakova gene: INTS1 was added
gene: INTS1 was added to Monogenic short stature. Sources: Expert Review Green,Literature
Mode of inheritance for gene: INTS1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: INTS1 were set to 28542170; 30622326; 31428919
Phenotypes for gene: INTS1 were set to Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies, OMIM:618571
Monogenic short stature v0.32 IGFALS Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.32 IGFALS Arina Puzriakova gene: IGFALS was added
gene: IGFALS was added to Monogenic short stature. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: IGFALS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IGFALS were set to 14762184; 16507628; 17726072; 18303074; 20591980; 21396577; 23488611; 24819402; 24423360; 27018247; 30717585; 36348166
Phenotypes for gene: IGFALS were set to Acid-labile subunit, deficiency of, OMIM:615961
Monogenic short stature v0.31 IGF2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.31 IGF2 Arina Puzriakova gene: IGF2 was added
gene: IGF2 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: IGF2 was set to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Publications for gene: IGF2 were set to 26154720
Phenotypes for gene: IGF2 were set to Silver-Russell syndrome 3, OMIM:616489
Monogenic short stature v0.30 IGF1R Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.30 IGF1R Arina Puzriakova gene: IGF1R was added
gene: IGF1R was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: IGF1R was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: IGF1R were set to Insulin-like growth factor I, resistance to, OMIM:270450
Monogenic short stature v0.29 IGF1 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.29 IGF1 Arina Puzriakova gene: IGF1 was added
gene: IGF1 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: IGF1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: IGF1 were set to Insulin-like growth factor I deficiency, OMIM:608747
Monogenic short stature v0.28 HRAS Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.28 HRAS Arina Puzriakova gene: HRAS was added
gene: HRAS was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: HRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: HRAS were set to 16170316; 16969868; 16443854; 21396583
Phenotypes for gene: HRAS were set to Costello syndrome, OMIM:218040
Mode of pathogenicity for gene: HRAS was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Monogenic short stature v0.27 HMGA2 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.27 HMGA2 Arina Puzriakova gene: HMGA2 was added
gene: HMGA2 was added to Monogenic short stature. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: HMGA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: HMGA2 were set to 29655892
Phenotypes for gene: HMGA2 were set to Silver-Russell syndrome 5, OMIM:618908
Monogenic short stature v0.26 GHR Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.26 GHR Arina Puzriakova gene: GHR was added
gene: GHR was added to Monogenic short stature. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: GHR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GHR were set to Laron dwarfism, OMIM:262500
Monogenic short stature v0.25 FGFR3 Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.25 FGFR3 Arina Puzriakova gene: FGFR3 was added
gene: FGFR3 was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: FGFR3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: FGFR3 were set to Hypochondroplasia, OMIM:146000; Crouzon syndrome with acanthosis nigricans, OMIM:612247; Thanatophoric dysplasia, type I, OMIM:187600; Thanatophoric dysplasia, type II, OMIM:187601
Monogenic short stature v0.24 FANCL Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.24 FANCL Arina Puzriakova gene: FANCL was added
gene: FANCL was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: FANCL was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FANCL were set to 16474160; 12724401; 25754594; 12973351; 19405097
Phenotypes for gene: FANCL were set to Fanconi anemia, complementation group L, OMIM:614083
Monogenic short stature v0.23 FANCI Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.23 FANCI Arina Puzriakova gene: FANCI was added
gene: FANCI was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: FANCI was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FANCI were set to 17452773; 11239453
Phenotypes for gene: FANCI were set to Fanconi anemia, complementation group I, OMIM:609053
Monogenic short stature v0.22 FANCG Arina Puzriakova Entity copied from Growth failure in early childhood v3.76
Monogenic short stature v0.22 FANCG Arina Puzriakova gene: FANCG was added
gene: FANCG was added to Monogenic short stature. Sources: Expert Review Green
Mode of inheritance for gene: FANCG was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FANCG were set to 16493006; 9806548
Phenotypes for gene: FANCG were set to Fanconi anemia, complementation group G, OMIM:614082
Monogenic short stature v0.21 FANCF Arina Puzriakova Entity copied from Growth failure in early childhood v3.76