myocardial infarction; stroke 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

22 genes associated with the disease myocardial infarction; stroke 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
ADD1 adducin 1 (alpha)
AGTR1 angiotensin II receptor, type 1
CETP cholesteryl ester transfer protein, plasma
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2J2 cytochrome P450, family 2, subfamily J, polypeptide 2
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
F13A1 coagulation factor XIII, A1 polypeptide
HMGCR 3-hydroxy-3-methylglutaryl-CoA reductase
IL1B interleukin 1, beta
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LDLR low density lipoprotein receptor
LIPC lipase, hepatic
NOS3 nitric oxide synthase 3 (endothelial cell)
P2RY12 purinergic receptor P2Y, G-protein coupled, 12
PCSK9 proprotein convertase subtilisin/kexin type 9
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1