branchial anomaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital developmental defect arising from the primitive branchial apparatus. (Human Phenotype Ontology, HP_0009794)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009794
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Genes

3 genes associated with the branchial anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
SIX1 SIX homeobox 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)