Aortic Valve Insufficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle. (Human Disease Ontology, DOID_57)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001022
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Genes

12 genes/proteins associated with the disease Aortic Valve Insufficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TIMP1 TIMP metallopeptidase inhibitor 1 2.88009
COL1A1 collagen, type I, alpha 1 2.88009
LOX lysyl oxidase 2.88009
NPPB natriuretic peptide B 2.88009
CTGF connective tissue growth factor 2.88009
TGFB2 transforming growth factor, beta 2 2.88009
TGFB1 transforming growth factor, beta 1 2.88009
FN1 fibronectin 1 2.88009
FSTL1 follistatin-like 1 2.88009
NPPA natriuretic peptide A 2.88009
COL3A1 collagen, type III, alpha 1 2.88009
HTR2B 5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled 1.19179