Primary Ovarian Insufficiency_Premature Ovarian Failure
Gene: NOGEnsemblGeneIds (GRCh38): ENSG00000183691
EnsemblGeneIds (GRCh37): ENSG00000183691
OMIM: 602991, Gene2Phenotype
NOG is in 7 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
Premature ovarian failure is not a prominent or common feature of proximal symphalangism. Only 2 cases have been reported with POI.Created: 11 Dec 2020, 6:02 a.m. | Last Modified: 11 Dec 2020, 6:02 a.m.
Panel Version: 0.153
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Symphalangism, proximal, 1A MIM#185800
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Red
- Genetic Health QLD
- Phenotypes
-
- Symphalangism, proximal, 1A MIM#185800
- OMIM
- 602991
- Clinvar variants
- Variants in NOG
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: nog has been classified as Red List (Low Evidence).
Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)Phenotypes for gene: NOG were changed from to Symphalangism, proximal, 1A MIM#185800
Set publications
Bryony Thompson (Royal Melbourne Hospital)Publications for gene: NOG were set to
Set mode of inheritance
Bryony Thompson (Royal Melbourne Hospital)Mode of inheritance for gene: NOG 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: NOG was added gene: NOG was added to Primary Ovarian Insufficiency_Premature Ovarian Failure. Sources: Genetic Health QLD Mode of inheritance for gene: NOG was set to Unknown