uterine hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of bleeding in the uterus; often in response to failed pregnancy (Mammalian Phenotype Ontology, MP_0004898)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004898
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Genes

5 gene mutations causing the uterine hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGA fibrinogen alpha chain
FGG fibrinogen gamma chain
FSHR follicle stimulating hormone receptor
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
PRDM1 PR domain containing 1, with ZNF domain