esophageal atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002032
Similar Terms
Downloads & Tools

Genes

11 genes associated with the esophageal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
EFTUD2 elongation factor Tu GTP binding domain containing 2
ERCC4 excision repair cross-complementation group 4
FGFR2 fibroblast growth factor receptor 2
HOXD13 homeobox D13
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SOX2 SRY (sex determining region Y)-box 2