abnormality of the right ventricle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the right ventricle of the heart. (Human Phenotype Ontology, HP_0001707)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001707
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11 genes associated with the abnormality of the right ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
BTK Bruton agammaglobulinemia tyrosine kinase
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FLNA filamin A, alpha
NOTCH1 notch 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
STAMBP STAM binding protein
VPS33B vacuolar protein sorting 33 homolog B (yeast)
WNT5A wingless-type MMTV integration site family, member 5A