Multiple Tumours
Gene: WT1EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 18 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:47 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- WAGR
- Denys-Drash Syndrome
- Frasier Syndrome Wilms tumor
- Gonadoblastoma
- Paediatric congenital malformation-dysmorphism-tumour syndromes
- OMIM
- 607102
- Clinvar variants
- Variants in WT1
- Penetrance
- Complete
- Panels with this gene
-
- Cytopenias and congenital anaemias
- Unexplained kidney failure in young people
- Sarcoma cancer susceptibility
- Intellectual disability
- Differences in sex development
- Structural eye disease
- Wilms tumour with features suggestive of predisposition
- Familial rhabdomyosarcoma
- Childhood solid tumours
- Adult solid tumours for rare disease
- Retinal disorders
- Sarcoma susceptibility
- Proteinuric renal disease
- Adult solid tumours cancer susceptibility
- DDG2P
- Glaucoma (developmental)
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
History Filter Activity
Set Mode of Inheritance, Added New Source
Ellen McDonagh (Genomics England Curator)WT1 was added to Multiple Tumourspanel. Source: Expert Review Green Model of inheritance for gene WT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Created
Ellen McDonagh (Genomics England Curator)WT1 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)WT1 was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)