abnormal uterine environment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly or inability of the uterus to support embryonic development (Mammalian Phenotype Ontology, MP_0004014)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004014
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Genes

29 gene mutations causing the abnormal uterine environment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
CALCRL calcitonin receptor-like
CBS cystathionine-beta-synthase
CENPB centromere protein B, 80kDa
DLGAP5 discs, large (Drosophila) homolog-associated protein 5
FGA fibrinogen alpha chain
FGFR2 fibroblast growth factor receptor 2
FKBP4 FK506 binding protein 4, 59kDa
FSHR follicle stimulating hormone receptor
FUT2 fucosyltransferase 2 (secretor status included)
HMX3 H6 family homeobox 3
HOXA11 homeobox A11
IL11RA interleukin 11 receptor, alpha
IL15 interleukin 15
IL6ST interleukin 6 signal transducer
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LIF leukemia inhibitory factor
NCOA1 nuclear receptor coactivator 1
PARL presenilin associated, rhomboid-like
PGR progesterone receptor
PRLR prolactin receptor
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SRC SRC proto-oncogene, non-receptor tyrosine kinase
TLR3 toll-like receptor 3
TSHR thyroid stimulating hormone receptor
TYROBP TYRO protein tyrosine kinase binding protein
WNT6 wingless-type MMTV integration site family, member 6