esophageal cancer Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A gastrointestinal system cancer that is located_in the esophagus. (Human Disease Ontology, DOID_5041)
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13 genes associated with the disease esophageal cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HECTD4 HECT domain containing E3 ubiquitin protein ligase 4 1.79724
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 1.53808
ADH1B alcohol dehydrogenase 1B (class I), beta polypeptide 1.52581
RUNX1 runt-related transcription factor 1 1.44218
ACAD10 acyl-CoA dehydrogenase family, member 10 1.40682
PLCE1 phospholipase C, epsilon 1 1.35663
PDE4D phosphodiesterase 4D, cAMP-specific 1.32252
RPL6 ribosomal protein L6 1.07383
UNC5CL unc-5 homolog C (C. elegans)-like 0.830123
ANP32A acidic (leucine-rich) nuclear phosphoprotein 32 family, member A 0.817078
CSNK1A1 casein kinase 1, alpha 1 0.561725
SEMA5B sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B 0.403461
NAALADL2 N-acetylated alpha-linked acidic dipeptidase-like 2 0.345945