primary ovarian insufficiency 19 Disease Ontology Browser

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Disease Ontology Browser

primary ovarian insufficiency 19 (DOID:0112278)
Alliance: disease page
Synonyms: POF19; POI19; premature ovarian failure 19
Alt IDs: OMIM:619245
Definition: A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22.

Disease References using Mouse Models (1)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Hsf2bpem2Amp/Hsf2bpem2Amp	involves: C57BL/6J * CBA/J	J:303558	View