esophageal disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A gastrointestinal system disease that is located_in the esophagus. (Human Disease Ontology, DOID_6050)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:6050
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Genes

22 genes associated with the disease esophageal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
CRTC1 CREB regulated transcription coactivator 1 0.88034
BARX1 BARX homeobox 1 0.824682
PTPDC1 protein tyrosine phosphatase domain containing 1 0.601958
ALDH1A2 aldehyde dehydrogenase 1 family, member A2 0.528352
SHROOM3 shroom family member 3 0.496271
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced 0.484681
ERICH5 glutamate-rich 5 0.474846
AGBL1 ATP/GTP binding protein-like 1 0.474846
GRID1 glutamate receptor, ionotropic, delta 1 0.474846
DSG1 desmoglein 1 0.473391
SNTB1 syntrophin, beta 1 (dystrophin-associated protein A1, 59kDa, basic component 1) 0.473391
FRMD3 FERM domain containing 3 0.469702
MFHAS1 malignant fibrous histiocytoma amplified sequence 1 0.453479
LECT1 leukocyte cell derived chemotaxin 1 0.445516
KHDRBS2 KH domain containing, RNA binding, signal transduction associated 2 0.443447
EPHB1 EPH receptor B1 0.432254
OSBPL10 oxysterol binding protein-like 10 0.426569
OTX2-AS1 OTX2 antisense RNA 1 (head to head) 0.422645
DSG3 desmoglein 3 0.42127
CAMTA1 calmodulin binding transcription activator 1 0.416099
HECW1 HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 0.412673
MIR99AHG mir-99a-let-7c cluster host gene 0.392682