This Panel is marked as Deleted
Kidneyome_SuperPanel_VCGS
Gene: WT1
WT1 (Wilms tumor 1)
EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 18 panels
EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 18 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- OMIM
- 607102
- Clinvar variants
- Variants in WT1
- Penetrance
- None
- Panels with this gene
-
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- 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
- Unexplained kidney failure in young people
- Intellectual disability
- Adult solid tumours cancer susceptibility
- Proteinuric renal disease
- Fetal anomalies
- DDG2P
- Glaucoma (developmental)
- Childhood solid tumours cancer susceptibility
History Filter Activity
28 Jan 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Eleanor Williams (Genomics England Curator)gene: WT1 was added gene: WT1 was added to Kidneyome_SuperPanel_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: WT1 was set to Unknown