Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1 		0.300 Biomarker disease CLINGEN
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.110 GeneticVariation disease CLINVAR
Entrez Id: 5892
Gene Symbol: RAD51D
RAD51D 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.110 CausalMutation disease CLINVAR In vivo measurement of the volume of distribution of water in cerebral grey matter: effects on the calculation of regional cerebral blood flow. 1548301 1992
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation disease CLINVAR In vivo measurement of the volume of distribution of water in cerebral grey matter: effects on the calculation of regional cerebral blood flow. 1548301 1992
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.110 GeneticVariation disease BEFREE Increasing recognition of the statistical burden posed by HNPCC (5 to 6 percent of all colorectal cancer) mandates that physicians have a better understanding of the genetics, natural history, and distinction between the hereditary site-specific variant (Lynch syndrome I) and the Cancer Family Syndrome (Lynch syndrome II). 3366037 1988
Entrez Id: 2052
Gene Symbol: EPHX1
EPHX1 		0.300 Biomarker disease 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 		0.600 CausalMutation disease CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065 1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT 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 		0.600 GeneticVariation disease UNIPROT Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515 1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 CausalMutation disease 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 		0.600 GeneticVariation disease UNIPROT Microsatellite instability and the role of hMSH2 in sporadic colorectalcancer. 8700523 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer. 8797773 1996
Entrez Id: 4437
Gene Symbol: MSH3
MSH3 		0.300 Biomarker disease CLINGEN hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA. 8805365 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. 8872463 1996
Entrez Id: 4437
Gene Symbol: MSH3
MSH3 		0.300 Biomarker disease CLINGEN hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6. 8942985 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria. 9048925 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Frequent somatic mutations of hMSH3 with reference to microsatellite instability in hereditary nonpolyposis colorectal cancers. 9240418 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. 9298827 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. 9311737 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds. 9419403 1997
Entrez Id: 999
Gene Symbol: CDH1
CDH1 		0.300 Biomarker disease CLINGEN E-cadherin germline mutations in familial gastric cancer. 9537325 1998
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627 1998