abnormal endometrium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the glandular mucous membrane lining of the uterine cavity that is hormonally responsive during the estrous/menstrual cycle and during pregnancy (Mammalian Phenotype Ontology, MP_0004896)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004896
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35 gene mutations causing the abnormal endometrium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSL4 acyl-CoA synthetase long-chain family member 4
AFP alpha-fetoprotein
ARID5B AT rich interactive domain 5B (MRF1-like)
BMPR1B bone morphogenetic protein receptor, type IB
BRCA1 breast cancer 1, early onset
CABLES1 Cdk5 and Abl enzyme substrate 1
CAV1 caveolin 1, caveolae protein, 22kDa
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CENPB centromere protein B, 80kDa
CHD2 chromodomain helicase DNA binding protein 2
CHST10 carbohydrate sulfotransferase 10
CSF1 colony stimulating factor 1 (macrophage)
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
EGR1 early growth response 1
ERRFI1 ERBB receptor feedback inhibitor 1
ESR1 estrogen receptor 1
FANCL Fanconi anemia, complementation group L
FSHR follicle stimulating hormone receptor
FZD1 frizzled class receptor 1
HOXA11 homeobox A11
IGF2R insulin-like growth factor 2 receptor
KPNA1 karyopherin alpha 1 (importin alpha 5)
LEPR leptin receptor
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
MCM8 minichromosome maintenance complex component 8
NPC1 Niemann-Pick disease, type C1
NPR2 natriuretic peptide receptor 2
PAX8 paired box 8
PGR progesterone receptor
PTEN phosphatase and tensin homolog
TIMP1 TIMP metallopeptidase inhibitor 1
WNT7A wingless-type MMTV integration site family, member 7A