esophagus squamous cell carcinoma Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. (Human Disease Ontology, DOID_3748)
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15 genes associated with the disease esophagus squamous cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
APOE apolipoprotein E 3.576
TOMM40 translocase of outer mitochondrial membrane 40 homolog (yeast) 2.39826
LPA lipoprotein, Lp(a) 2.21675
LDLR low density lipoprotein receptor 2.14896
DNAH11 dynein, axonemal, heavy chain 11 1.8787
LRFN2 leucine rich repeat and fibronectin type III domain containing 2 1.69467
HMGCR 3-hydroxy-3-methylglutaryl-CoA reductase 1.49655
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8 1.40698
SLCO1B1 solute carrier organic anion transporter family, member 1B1 1.34719
APOC1 apolipoprotein C-I 1.01598
FBXO11 F-box protein 11 0.774314
CETP cholesteryl ester transfer protein, plasma 0.764084
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2 0.694381
PLCXD2 phosphatidylinositol-specific phospholipase C, X domain containing 2 0.636511
RELN reelin 0.510444