Tricuspid Valve Stenosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A tricuspid valve disease that is characterized by the narrowing of the orifice of the tricuspid valve of the heart. This causes increased resistance to blood flow through the valve. (Human Disease Ontology, DOID_4078)
External Link https://www.disgenet.org/browser/0/1/0/C0040963
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Genes

26 genes associated with the disease Tricuspid Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTSL2 ADAMTS-like 2
AMELX amelogenin, X-linked
C1QBP complement component 1, q subcomponent binding protein
CD8A CD8a molecule
CDX2 caudal type homeobox 2
CHPT1 choline phosphotransferase 1
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
DHDDS dehydrodolichyl diphosphate synthase
GH1 growth hormone 1
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
GRHL3 grainyhead-like 3 (Drosophila)
GSK3B glycogen synthase kinase 3 beta
HEXDC hexosaminidase (glycosyl hydrolase family 20, catalytic domain) containing
ING2 inhibitor of growth family, member 2
OGA O-GlcNAcase
PEX13 peroxisomal biogenesis factor 13
RPGRIP1L RPGRIP1-like
SHOX short stature homeobox
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SPINT1 serine peptidase inhibitor, Kunitz type 1
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TESC tescalcin
TP53 tumor protein p53
TSC1 tuberous sclerosis 1
TYMS thymidylate synthetase
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor