Primary Ovarian Insufficiency_Premature Ovarian Failure
Gene: ZP3EnsemblGeneIds (GRCh38): ENSG00000188372
EnsemblGeneIds (GRCh37): ENSG00000188372
OMIM: 182889, Gene2Phenotype
ZP3 is in 2 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Oocyte maturation defect but with normal ovarian reserves and menstrual cycles.Created: 11 Dec 2020, 1:42 a.m. | Last Modified: 11 Dec 2020, 1:42 a.m.
Panel Version: 0.87
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Oocyte maturation defect 3, MIM# 617712
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Red
- Genetic Health QLD
- Phenotypes
-
- Oocyte maturation defect 3, MIM# 617712
- OMIM
- 182889
- Clinvar variants
- Variants in ZP3
- 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: zp3 has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: ZP3 were changed from to Oocyte maturation defect 3, MIM# 617712
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: ZP3 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: ZP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Created, Added New Source, Set mode of inheritance
Bryony Thompson (Royal Melbourne Hospital)gene: ZP3 was added gene: ZP3 was added to Primary Ovarian Insufficiency_Premature Ovarian Failure. Sources: Genetic Health QLD Mode of inheritance for gene: ZP3 was set to Unknown