vascular disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart. (Human Disease Ontology, DOID_178)
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29 genes involed in the disease vascular 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
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
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)
F12 coagulation factor XII (Hageman factor)
FBN1 fibrillin 1
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
ITPKC inositol-trisphosphate 3-kinase C
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
SCN9A sodium channel, voltage gated, type IX alpha subunit
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
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)