abnormality of the aortic arch Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the arch of aorta. (Human Phenotype Ontology, HP_0012303)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012303
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Genes

9 genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
CREBBP CREB binding protein
CRELD1 cysteine-rich with EGF-like domains 1
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
GATA6 GATA binding protein 6
GLI3 GLI family zinc finger 3
PIK3R2 phosphoinositide-3-kinase, regulatory subunit 2 (beta)
STRA6 stimulated by retinoic acid 6
TBX1 T-box 1