Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 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: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. 7557107 1995
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC) 7757073 1995
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 CausalMutation group CLINVAR Mismatch repair deficiency in phenotypically normal human cells. 7632227 1995
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 Biomarker group CLINGEN GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells. 7604265 1995
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 Biomarker group CLINGEN Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells. 7604264 1995
Entrez Id: 324
Gene Symbol: APC
APC 		0.300 Biomarker group CTD_human The molecular basis of Turcot's syndrome. 7661930 1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR RNA-based mutation screening in hereditary nonpolyposis colorectal cancer. 8808596 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. 8574961 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. 8566964 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 Biomarker group CLINGEN Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice. 8706033 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Genetic heterogeneity and unmapped genes for colorectal cancer. 8640829 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. 8872463 1996
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 CausalMutation group CLINVAR DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. 8776590 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Genetic counseling in a Navajo hereditary nonpolyposis colorectal cancer kindred. 8630936 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. 8574961 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer. 8797773 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. 8566964 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. 8776590 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome. 8880570 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. 8776590 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome. 8646682 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. 8574961 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. 8872463 1996
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16. 8571956 1996