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
-
- Intellectual disability
- Sarcoma cancer susceptibility
- Differences in sex development
- Cytopenias and congenital anaemias
- Fetal anomalies
- Wilms tumour with features suggestive of predisposition
- Structural eye disease
- Familial rhabdomyosarcoma
- Childhood solid tumours
- Adult solid tumours for rare disease
- Sarcoma susceptibility
- Unexplained kidney failure in young people
- Adult solid tumours cancer susceptibility
- Proteinuric renal disease
- DDG2P
- Retinal disorders
- Glaucoma (developmental)
- 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)