aortic disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An artery disease that is characterized by degeneration of the cells composing the aortic wall. (Human Disease Ontology, DOID_520)
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Genes

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

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
COL3A1 collagen, type III, alpha 1
FBN1 fibrillin 1
MYH11 myosin, heavy chain 11, smooth muscle
MYLK myosin light chain kinase
PRKG1 protein kinase, cGMP-dependent, type I
SMAD3 SMAD family member 3
TGFB2 transforming growth factor, beta 2
TGFBR1 transforming growth factor, beta receptor 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)