myocardial ischemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. (Human Disease Ontology, DOID_3393)
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Genes

18 genes associated with the disease myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
APOA1 apolipoprotein A-I
APOB apolipoprotein B
APOE apolipoprotein E
CD14 CD14 molecule
CETP cholesteryl ester transfer protein, plasma
F13A1 coagulation factor XIII, A1 polypeptide
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LIPC lipase, hepatic
LPL lipoprotein lipase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PCSK9 proprotein convertase subtilisin/kexin type 9
PON1 paraoxonase 1