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 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 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 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 Familial endometrial cancer in female carriers of MSH6 germline mutations. 10508506 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: 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 Germ-line msh6 mutations in colorectal cancer families. 10537275 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 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 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 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: 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: 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 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 MSH6 germline mutations are rare in colorectal cancer families. 14520694 2003
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: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 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 UNIPROT Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue. 14974087 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