abnormality of the tricuspid valve Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the tricuspid valve. (Human Phenotype Ontology, HP_0001702)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001702
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19 genes associated with the abnormality of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
CCDC22 coiled-coil domain containing 22
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COMT catechol-O-methyltransferase
COX7B cytochrome c oxidase subunit VIIb
FBN1 fibrillin 1
FLNA filamin A, alpha
GP1BB glycoprotein Ib (platelet), beta polypeptide
HCCS holocytochrome c synthase
HIRA histone cell cycle regulator
KIAA0196 KIAA0196
MYH7 myosin, heavy chain 7, cardiac muscle, beta
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SCN5A sodium channel, voltage gated, type V alpha subunit
TBX1 T-box 1
UFD1L ubiquitin fusion degradation 1 like (yeast)