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
Similar Terms
Downloads & Tools

Genes

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