Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 Biomarker group MGD
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 Biomarker group MGD
Entrez Id: 4072
Gene Symbol: EPCAM
EPCAM 		0.410 GeneticVariation group CLINVAR
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1 		0.300 Biomarker group CLINGEN
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR [A method of study for stomatological materials]. 1061282 1976
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 CausalMutation group CLINVAR Review of the basic principles of drug action. 2440087 1986
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group CLINVAR Immunosuppression. Binding by design. 1710317 1991
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Oxidative metabolism in reperfused myocardium. 1756143 1991
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 CausalMutation group CLINVAR """Central arousal"" and sexual responsiveness in the snail, Helix aspersa." 2059188 1991
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation group CLINVAR """Central arousal"" and sexual responsiveness in the snail, Helix aspersa." 2059188 1991
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515 1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 Biomarker group CLINGEN Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515 1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. 8062247 1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group CLINVAR hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. 8062247 1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development. 7874129 1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group CLINVAR Genetic instability in human ovarian cancer cell lines. 7937795 1994
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Mutation of a mutL homolog in hereditary colon cancer. 8128251 1994
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 Biomarker group CLINGEN Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. 8072530 1994
Entrez Id: 2052
Gene Symbol: EPHX1
EPHX1 		0.300 Biomarker group CLINGEN Human microsomal epoxide hydrolase: genetic polymorphism and functional expression in vitro of amino acid variants. 7516776 1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients. 8581513 1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes. 8592341 1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065 1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. 7726159 1995
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families. 8521398 1995
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Alternative splicing of MLH1 messenger RNA in human normal cells. 7728749 1995