Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.610 GeneticVariation UNIPROT A dominant negative mutation of transforming growth factor-beta receptor type II gene in microsatellite stable oesophageal carcinoma. 10789724

2000
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.610 CausalMutation CGI

Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.500 CausalMutation CGI

Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.500 GeneticVariation UNIPROT

Entrez Id: 1956
Gene Symbol: EGFR
EGFR
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.500 CausalMutation CGI

Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.410 CausalMutation CGI

Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.400 CausalMutation CGI

Entrez Id: 49860
Gene Symbol: CRNN
CRNN
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.320 GeneticVariation UNIPROT Genetic variants of C1orf10 and risk of esophageal squamous cell carcinoma in a Chinese population. 19558548

2009
Entrez Id: 11178
Gene Symbol: LZTS1
LZTS1
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.300 CausalMutation CGI