Primary Ovarian Insufficiency_Premature Ovarian Failure
Gene: ZP1EnsemblGeneIds (GRCh38): ENSG00000149506
EnsemblGeneIds (GRCh37): ENSG00000149506
OMIM: 195000, Gene2Phenotype
ZP1 is in 2 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Presents as primary infertility rather than POI/POF.Created: 11 Dec 2020, 1:59 a.m. | Last Modified: 11 Dec 2020, 1:59 a.m.
Panel Version: 0.93
Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Oocyte maturation defect 1, MIM# 615774
Publications
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Expert Review Red
- Genetic Health QLD
- Phenotypes
-
- Oocyte maturation defect 1, MIM# 615774
- OMIM
- 195000
- Clinvar variants
- Variants in ZP1
- 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: zp1 has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: ZP1 were changed from to Oocyte maturation defect 1, MIM# 615774
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: ZP1 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: ZP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Bryony Thompson (Royal Melbourne Hospital)gene: ZP1 was added gene: ZP1 was added to Primary Ovarian Insufficiency_Premature Ovarian Failure. Sources: Genetic Health QLD Mode of inheritance for gene: ZP1 was set to Unknown