coronary artery disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
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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19 genes associated with the disease coronary artery disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PHACTR1 phosphatase and actin regulator 1 1.45255
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2 0.825265
MRPS6 mitochondrial ribosomal protein S6 0.745324
MIA3 melanoma inhibitory activity family, member 3 0.63207
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 0.602429
CXCL12 chemokine (C-X-C motif) ligand 12 0.544585
WDR12 WD repeat domain 12 0.52461
C12ORF42 chromosome 12 open reading frame 42 0.403461
MARC1 mitochondrial amidoxime reducing component 1 0.345945
RCSD1 RCSD domain containing 1 0.311576
SLC22A3 solute carrier family 22 (organic cation transporter), member 3 0.297866
CLEC14A C-type lectin domain family 14, member A 0.264872
COL4A2 collagen, type IV, alpha 2 0.264872
TENM1 teneurin transmembrane protein 1 0.197766
PPP4R2 protein phosphatase 4, regulatory subunit 2 0.197766
LZTS1 leucine zipper, putative tumor suppressor 1 0.15771
LTA lymphotoxin alpha 0.15771
SETBP1 SET binding protein 1 0.126165
ADAMTS7 ADAM metallopeptidase with thrombospondin type 1 motif, 7 0.064973