artery disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A vascular disease that is located_in an artery. (Human Disease Ontology, DOID_0050828)
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Genes

21 genes involed in the disease artery disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ACTA2 actin, alpha 2, smooth muscle, aorta
APOA1 apolipoprotein A-I
APOB apolipoprotein B
APOBR apolipoprotein B receptor
CETP cholesteryl ester transfer protein, plasma
COL3A1 collagen, type III, alpha 1
CORIN corin, serine peptidase
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
FBN1 fibrillin 1
LDLRAP1 low density lipoprotein receptor adaptor protein 1
LPA lipoprotein, Lp(a)
MYH11 myosin, heavy chain 11, smooth muscle
MYLK myosin light chain kinase
PRKG1 protein kinase, cGMP-dependent, type I
RSAD2 radical S-adenosyl methionine domain containing 2
SMAD3 SMAD family member 3
STOX1 storkhead box 1
TGFB2 transforming growth factor, beta 2
TGFBR1 transforming growth factor, beta receptor 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)