coronary artery disease; myocardial infarction Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group cardiovascular (Genetic Association Database)
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Genes

30 genes associated with the disease coronary artery disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ALOX5AP arachidonate 5-lipoxygenase-activating protein
APOA1 apolipoprotein A-I
BRINP3 bone morphogenetic protein/retinoic acid inducible neural-specific 3
CD14 CD14 molecule
CETP cholesteryl ester transfer protein, plasma
CX3CR1 chemokine (C-X3-C motif) receptor 1
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HMGCR 3-hydroxy-3-methylglutaryl-CoA reductase
HMOX1 heme oxygenase 1
ICAM1 intercellular adhesion molecule 1
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
KIAA0391 KIAA0391
LRP8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor
MTHFD1L methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPR1 natriuretic peptide receptor 1
PON1 paraoxonase 1
PSMA6 proteasome (prosome, macropain) subunit, alpha type, 6
REN renin
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SOD2 superoxide dismutase 2, mitochondrial
SOD3 superoxide dismutase 3, extracellular