Additional findings_Adult
Gene: WT1
WT1 (Wilms tumor 1)
EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 13 panels
EnsemblGeneIds (GRCh38): ENSG00000184937
EnsemblGeneIds (GRCh37): ENSG00000184937
OMIM: 607102, Gene2Phenotype
WT1 is in 13 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Wilms' tumor MIM#194070
- OMIM
- 607102
- Clinvar variants
- Variants in WT1
- Penetrance
- None
- Publications
- Panels with this gene
-
- Incidentalome
- Additional findings_Adult
- Fetal anomalies
- Additional findings_Paediatric
- Incidentalome_PREGEN_DRAFT
- Proteinuria
- Congenital diaphragmatic hernia
- BabyScreen+ newborn screening
- Wilms Tumour
- Transplant Co-Morbidity Superpanel
- Differences of Sex Development
- Cancer Predisposition_Paediatric
- Primary Ovarian Insufficiency_Premature Ovarian Failure
History Filter Activity
4 Jun 2023, Gel status: 3
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: wt1 has been classified as Green List (High Evidence).
4 Jun 2023, Gel status: 3
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: wt1 has been classified as Green List (High Evidence).
4 Jun 2023, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: WT1 was added gene: WT1 was added to Additional findings_Adult. Sources: Expert list Mode of inheritance for gene: WT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: WT1 were set to 35802134 Phenotypes for gene: WT1 were set to Wilms' tumor MIM#194070 gene: WT1 was marked as current diagnostic