pulmonary artery stenosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal narrowing or constriction of the pulmonary artery, in the main pulmonary artery and/or in the left or right pulmonary artery branches. (Human Phenotype Ontology, HP_0004415)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004415
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13 genes associated with the pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARHGAP31 Rho GTPase activating protein 31
ELN elastin
GPC6 glypican 6
IFT43 intraflagellar transport 43
JAG1 jagged 1
LTBP4 latent transforming growth factor beta binding protein 4
MGP matrix Gla protein
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NKX2-5 NK2 homeobox 5
NOTCH2 notch 2
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
ZEB2 zinc finger E-box binding homeobox 2