Primary Ovarian Insufficiency_Premature Ovarian Failure
Gene: WEE2EnsemblGeneIds (GRCh38): ENSG00000214102
EnsemblGeneIds (GRCh37): ENSG00000214102
OMIM: 614084, Gene2Phenotype
WEE2 is in 2 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Over 10 individuals reported, however presentation is with primary infertility rather than POI/POF.Created: 11 Dec 2020, 4:18 a.m. | Last Modified: 11 Dec 2020, 4:18 a.m.
Panel Version: 0.109
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Oocyte maturation defect 5, MIM# 617996
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Red
- Genetic Health QLD
- Phenotypes
-
- Oocyte maturation defect 5, MIM# 617996
- OMIM
- 614084
- Clinvar variants
- Variants in WEE2
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: wee2 has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: WEE2 were changed from to Oocyte maturation defect 5, MIM# 617996
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: WEE2 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: WEE2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Bryony Thompson (Royal Melbourne Hospital)gene: WEE2 was added gene: WEE2 was added to Primary Ovarian Insufficiency_Premature Ovarian Failure. Sources: Genetic Health QLD Mode of inheritance for gene: WEE2 was set to Unknown