esophageal disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A gastrointestinal system disease that is located_in the esophagus. (Human Disease Ontology, DOID_6050)
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Genes

9 genes associated with the disease esophageal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TSLP thymic stromal lymphopoietin 0.58494
WDR36 WD repeat domain 36 0.345945
PRIM2 primase, DNA, polypeptide 2 (58kDa) 0.256228
SHROOM3 shroom family member 3 0.256228
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced 0.197766
ERICH5 glutamate-rich 5 0.080593
SNTB1 syntrophin, beta 1 (dystrophin-associated protein A1, 59kDa, basic component 1) 0.064973
DSG1 desmoglein 1 0.064973
NRG3 neuregulin 3 0.043246