coronary disease; 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

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

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ARG1 arginase 1
CTCF CCCTC-binding factor (zinc finger protein)
DNAH11 dynein, axonemal, heavy chain 11
FADS2 fatty acid desaturase 2
FADS3 fatty acid desaturase 3
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HSPA1A heat shock 70kDa protein 1A
LDLR low density lipoprotein receptor
LIPG lipase, endothelial
MADD MAP-kinase activating death domain
MMP1 matrix metallopeptidase 1
MMP3 matrix metallopeptidase 3
MMP9 matrix metallopeptidase 9
NQO1 NAD(P)H dehydrogenase, quinone 1
PRMT8 protein arginine methyltransferase 8
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
TMEM57 transmembrane protein 57
TNF tumor necrosis factor