ovary atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of the ovaries associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes (Mammalian Phenotype Ontology, MP_0004833)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004833
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13 gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CCDC169-SOHLH2 CCDC169-SOHLH2 readthrough
CDK2 cyclin-dependent kinase 2
FSHR follicle stimulating hormone receptor
HELQ helicase, POLQ-like
KL klotho
MAD2L2 MAD2 mitotic arrest deficient-like 2 (yeast)
MCPH1 microcephalin 1
NOBOX NOBOX oogenesis homeobox
PROKR2 prokineticin receptor 2
PTPN6 protein tyrosine phosphatase, non-receptor type 6
RAD21L1 RAD21-like 1 (S. pombe)
SAFB scaffold attachment factor B