double outlet right ventricle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_6406)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001719
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Genes

9 genes associated with the double outlet right ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CFC1 cripto, FRL-1, cryptic family 1
CHD7 chromodomain helicase DNA binding protein 7
GATA6 GATA binding protein 6
GDF1 growth differentiation factor 1
KIAA0196 KIAA0196
NKX2-5 NK2 homeobox 5
NKX2-6 NK2 homeobox 6
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
TBX1 T-box 1
Funding