uterus atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of the uterus 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_0004894)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004894
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Genes

9 gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CDK2 cyclin-dependent kinase 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
FSHR follicle stimulating hormone receptor
KL klotho
LHX9 LIM homeobox 9
NPC1 Niemann-Pick disease, type C1
PROKR2 prokineticin receptor 2