gastrointestinal 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:0002589
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Genes

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

Symbol Name
CEP57 centrosomal protein 57kDa
CHD7 chromodomain helicase DNA binding protein 7
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
EFTUD2 elongation factor Tu GTP binding domain containing 2
ERCC4 excision repair cross-complementation group 4
FGFR2 fibroblast growth factor receptor 2
FOXF1 forkhead box F1
HOXD13 homeobox D13
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NEK1 NIMA-related kinase 1
RFX6 regulatory factor X, 6
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SALL1 spalt-like transcription factor 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SOX2 SRY (sex determining region Y)-box 2