Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.700 CausalMutation disease CLINVAR
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
0.610 CausalMutation disease CLINVAR
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
0.610 Biomarker disease CTD_human
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
0.610 CausalMutation disease CGI
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
0.600 CausalMutation disease CLINVAR
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
0.600 CausalMutation disease CGI
Entrez Id: 1956
Gene Symbol: EGFR
EGFR
0.600 CausalMutation disease CGI
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
0.500 Biomarker disease CTD_human
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
0.500 CausalMutation disease CGI
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.500 Biomarker disease CTD_human
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.500 CausalMutation disease CGI
Entrez Id: 11178
Gene Symbol: LZTS1
LZTS1
0.500 Biomarker disease CTD_human
Entrez Id: 11178
Gene Symbol: LZTS1
LZTS1
0.500 CausalMutation disease CGI
Entrez Id: 26272
Gene Symbol: FBXO4
FBXO4
0.300 GeneticVariation disease UNIPROT
Entrez Id: 7039
Gene Symbol: TGFA
TGFA
0.010 Biomarker disease BEFREE A model system for tumor angiogenesis: involvement of transforming growth factor-alpha in tube formation of human microvascular endothelial cells induced by esophageal cancer cells. 1380804 1992
Entrez Id: 4953
Gene Symbol: ODC1
ODC1
0.020 AlteredExpression disease BEFREE Mechanisms sustaining high ODC mRNA levels in esophageal cancers may be an enhancement of the promoter activity of this gene or stabilization of the mRNA. 1423312 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.700 GeneticVariation disease BEFREE Mutations in exons 5-8 of the p53 gene were investigated by PCR-SSCP analysis using 10(3) sorted nuclei obtained from each endoscopic biopsy specimen of 16 patients with esophageal cancer. 1483940 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.700 GeneticVariation disease BEFREE Mutations of the p53 gene were found in 5 cases of gastric cancer and 4 cases of esophageal cancer. 1499939 1992
Entrez Id: 57508
Gene Symbol: INTS2
INTS2
0.020 GeneticVariation disease BEFREE Amplification of the hst-1 and int-2 genes on chromosome 11q13 has previously been found in over 20% of human primary esophageal cancers. 1533816 1992
Entrez Id: 2249
Gene Symbol: FGF4
FGF4
0.020 GeneticVariation disease BEFREE Amplification of the hst-1 and int-2 genes on chromosome 11q13 has previously been found in over 20% of human primary esophageal cancers. 1533816 1992
Entrez Id: 2248
Gene Symbol: FGF3
FGF3
0.020 GeneticVariation disease BEFREE Amplification of the hst-1 and int-2 genes on chromosome 11q13 has previously been found in over 20% of human primary esophageal cancers. 1533816 1992
Entrez Id: 324
Gene Symbol: APC
APC
0.070 GeneticVariation disease BEFREE These data suggest that loss of heterozygosity of regions on 5q including the APC and MCC genetic loci is involved in the development and/or progression of most human esophageal cancers. 1565631 1992
Entrez Id: 4163
Gene Symbol: MCC
MCC
0.010 GeneticVariation disease BEFREE These data suggest that loss of heterozygosity of regions on 5q including the APC and MCC genetic loci is involved in the development and/or progression of most human esophageal cancers. 1565631 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.700 GeneticVariation disease BEFREE Archival analysis of p53 genetic and protein alterations in Chinese esophageal cancer. 1923503 1991
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.700 Biomarker disease BEFREE However, the finding of p53 mutations in Barrett's epithelium adjacent to adenocarcinomas may have clinical implications for p53 as a premalignant marker for esophageal cancer. 1943188 1991