abnormal uterus physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the female muscular organ of gestation in which the developing embryo or fetus is nourished until birth (Mammalian Phenotype Ontology, MP_0009671)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009671
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21 gene mutations causing the abnormal uterus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ACSL4 acyl-CoA synthetase long-chain family member 4
ADM adrenomedullin
ANTXR2 anthrax toxin receptor 2
CALCRL calcitonin receptor-like
CAV1 caveolin 1, caveolae protein, 22kDa
EPHA1 EPH receptor A1
ESR1 estrogen receptor 1
FGA fibrinogen alpha chain
FGG fibrinogen gamma chain
FSHR follicle stimulating hormone receptor
IFNG interferon, gamma
IFNGR1 interferon gamma receptor 1
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
NR1H2 nuclear receptor subfamily 1, group H, member 2
NR4A1 nuclear receptor subfamily 4, group A, member 1
PGR progesterone receptor
PRDM1 PR domain containing 1, with ZNF domain
TLR3 toll-like receptor 3
TP63 tumor protein p63
TYROBP TYRO protein tyrosine kinase binding protein