Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 Biomarker disease CTD_human
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Endometrial cancer in four sisters: report of a kindred with presumed cancer family syndrome. 8063241 1994
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation disease CLINVAR Endometrial cancer in four sisters: report of a kindred with presumed cancer family syndrome. 8063241 1994
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. 9354786 1997
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. 10521294 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer. 9929971 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Germ-line msh6 mutations in colorectal cancer families. 10537275 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Familial endometrial cancer in female carriers of MSH6 germline mutations. 10508506 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer. 10480359 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Germ-line msh6 mutations in colorectal cancer families. 10537275 1999
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation disease CLINVAR Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer. 9929971 1999
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation disease CLINVAR Germ-line msh6 mutations in colorectal cancer families. 10537275 1999
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation disease CLINVAR Familial endometrial cancer in female carriers of MSH6 germline mutations. 10508506 1999
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation disease CLINVAR Germ-line msh6 mutations in colorectal cancer families. 10537275 1999
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT A role for MLH3 in hereditary nonpolyposis colorectal cancer. 11586295 2001
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. 12732731 2003
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR MSH6 germline mutations are rare in colorectal cancer families. 14520694 2003
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. 12658575 2003
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation disease CLINVAR MSH6 germline mutations are rare in colorectal cancer families. 14520694 2003
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation disease CLINVAR Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. 12732731 2003
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease UNIPROT Germline mutations in MLH1, MSH2 and MSH6 in Korean hereditary non-polyposis colorectal cancer families. 15365995 2004
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. 14961575 2004
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. 15236168 2004
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. 15236168 2004