Gastrointestinal Hemorrhage Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage affecting the gastrointestinal tract. (Human Phenotype Ontology, HP_0002239)
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Genes

21 genes associated with the Gastrointestinal Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
CYP4F11 cytochrome P450, family 4, subfamily F, polypeptide 11
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
GSTP1 glutathione S-transferase pi 1
HFE hemochromatosis
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMOX1 heme oxygenase 1
ICAM1 intercellular adhesion molecule 1
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KDR kinase insert domain receptor
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
TGFB1 transforming growth factor, beta 1
VEGFA vascular endothelial growth factor A
VKORC1 vitamin K epoxide reductase complex, subunit 1