Tricuspid Valve Insufficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the opposite direction to normal. (Human Disease Ontology, DOID_4080)
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Genes

6 genes associated with the Tricuspid Valve Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADORA2B adenosine A2b receptor
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
GALNT13 polypeptide N-acetylgalactosaminyltransferase 13
HBA1 hemoglobin, alpha 1
HBB hemoglobin, beta