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Intellectual disability syndromic and non-syndromic

Gene: WDR37

Green List (high evidence)

WDR37 (WD repeat domain 37)
EnsemblGeneIds (GRCh38): ENSG00000047056
EnsemblGeneIds (GRCh37): ENSG00000047056
WDR37 is in 7 panels

1 review

Chirag Patel (Genetic Health Queensland)

Green List (high evidence)

9 unrelated patients reported, with functional studies.
Created: 4 Dec 2019, 10:15 p.m. | Last Modified: 4 Dec 2019, 10:15 p.m.
Panel Version: 0.349
Sources: Expert list
Created: 4 Dec 2019, 10:14 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Neurooculocardiogenitourinary syndrome; OMIM #618652

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Neurooculocardiogenitourinary syndrome
  • OMIM #618652
Clinvar variants
Variants in WDR37
Penetrance
None
Publications
Panels with this gene

History Filter Activity

14 Jan 2020, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: wdr37 has been classified as Green List (High Evidence).

4 Dec 2019, Gel status: 3

Entity classified by Genomics England curator

Chirag Patel (Genetic Health Queensland)

Gene: wdr37 has been classified as Green List (High Evidence).

4 Dec 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Chirag Patel (Genetic Health Queensland)

gene: WDR37 was added gene: WDR37 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list Mode of inheritance for gene: WDR37 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: WDR37 were set to PubMed: 31327508; 31327510 Phenotypes for gene: WDR37 were set to Neurooculocardiogenitourinary syndrome; OMIM #618652 Review for gene: WDR37 was set to GREEN