Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 Biomarker MGD

Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 Biomarker MGD

Entrez Id: 4072
Gene Symbol: EPCAM
EPCAM
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.410 GeneticVariation CLINVAR

Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.300 Biomarker CLINGEN

Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 CausalMutation CLINVAR [A method of study for stomatological materials]. 1061282

1976
Entrez Id: 5395
Gene Symbol: PMS2
PMS2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.640 CausalMutation CLINVAR Review of the basic principles of drug action. 2440087

1986
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 GeneticVariation CLINVAR Immunosuppression. Binding by design. 1710317

1991
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 CausalMutation CLINVAR Oxidative metabolism in reperfused myocardium. 1756143

1991
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.640 CausalMutation CLINVAR """Central arousal"" and sexual responsiveness in the snail, Helix aspersa." 2059188

1991
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.100 CausalMutation CLINVAR """Central arousal"" and sexual responsiveness in the snail, Helix aspersa." 2059188

1991
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation CLINVAR Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515

1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 Biomarker CLINGEN Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515

1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation CLINVAR hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. 8062247

1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 GeneticVariation CLINVAR hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. 8062247

1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation 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
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 GeneticVariation CLINVAR Genetic instability in human ovarian cancer cell lines. 7937795

1994
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 CausalMutation CLINVAR Mutation of a mutL homolog in hereditary colon cancer. 8128251

1994
Entrez Id: 5395
Gene Symbol: PMS2
PMS2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.640 Biomarker CLINGEN Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. 8072530

1994
Entrez Id: 2052
Gene Symbol: EPHX1
EPHX1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.300 Biomarker 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
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation 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
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation 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
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065

1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation CLINVAR Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. 7726159

1995
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 CausalMutation CLINVAR Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families. 8521398

1995
Entrez Id: 4292
Gene Symbol: MLH1
MLH1
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.700 CausalMutation CLINVAR Alternative splicing of MLH1 messenger RNA in human normal cells. 7728749

1995