patent foramen ovale Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001655
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Genes

10 genes associated with the patent foramen ovale phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GAT3 beta-1,3-glucuronyltransferase 3
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
COL11A1 collagen, type XI, alpha 1
DSE dermatan sulfate epimerase
GATA6 GATA binding protein 6
LTBP4 latent transforming growth factor beta binding protein 4
PHGDH phosphoglycerate dehydrogenase
STAMBP STAM binding protein
TBX20 T-box 20
TSFM Ts translation elongation factor, mitochondrial