Incidentalome_PREGEN_DRAFT
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
1 review
Tony Roscioli (New South Wales Health Pathology)
A clear cause of an early onset Mendelian disorder - should be removed from this panelCreated: 7 Jan 2021, 1:01 a.m. | Last Modified: 7 Jan 2021, 1:01 a.m.
Panel Version: 0.7
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- NSW Health Pathology
- OMIM
- 607102
- Clinvar variants
- Variants in WT1
- Penetrance
- None
- 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
7 Jan 2021, Gel status: 1
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: wt1 has been classified as Red List (Low Evidence).
7 Jan 2021, Gel status: 1
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: wt1 has been classified as Red List (Low Evidence).
9 Nov 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: WT1 was added gene: WT1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: WT1 was set to Unknown