Esophageal cancer Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A gastrointestinal system cancer that is located_in the esophagus. (Human Disease Ontology, DOID_5041)
External Link https://www.ebi.ac.uk/gwas/search?query=Esophageal cancer
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Genes

9 genes associated with the Esophageal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HECTD4 HECT domain containing E3 ubiquitin protein ligase 4 1.30208
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 1.15711
ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide 1.14772
RUNX1 runt-related transcription factor 1 1.09468
ACAD10 acyl-CoA dehydrogenase family, member 10 1.0654
PLCE1 phospholipase C, epsilon 1 1.03855
PDE4D phosphodiesterase 4D, cAMP-specific 1.01293
CSNK1A1 casein kinase 1, alpha 1 0.463473
SEMA5B sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B 0.342586