Uterine Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

29 genes associated with the Uterine Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AGTR1 angiotensin II receptor, type 1
AGTR2 angiotensin II receptor, type 2
AHRR aryl-hydrocarbon receptor repressor
C10ORF55 chromosome 10 open reading frame 55
CCL2 chemokine (C-C motif) ligand 2
CETP cholesteryl ester transfer protein, plasma
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
COMT catechol-O-methyltransferase
CPB2 carboxypeptidase B2 (plasma)
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
GSTM1 glutathione S-transferase mu 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HSD17B1 hydroxysteroid (17-beta) dehydrogenase 1
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
IL10 interleukin 10
IL1B interleukin 1, beta
IL6 interleukin 6
IRS2 insulin receptor substrate 2
MMP2 matrix metallopeptidase 2
MMP9 matrix metallopeptidase 9
PGR progesterone receptor
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
TIMP2 TIMP metallopeptidase inhibitor 2