uterus cysts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of fluid-filled structures inside the lumen of the uterus; usually refers to benign growths (Mammalian Phenotype Ontology, MP_0009082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009082
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9 gene mutations causing the uterus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
CAV1 caveolin 1, caveolae protein, 22kDa
CHD2 chromodomain helicase DNA binding protein 2
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DRD2 dopamine receptor D2
ESR1 estrogen receptor 1
FSHR follicle stimulating hormone receptor
HOXA10 homeobox A10