MSH6
From SNPedia
| is a | gene |
| is | mentioned by |
| Full name | mutS homolog 6 (E. coli) |
| EntrezGene | 2956 |
| PheGenI | 2956 |
| VariationViewer | 2956 |
| ClinVar | MSH6 |
| GeneCards | MSH6 |
| dbSNP | 2956 |
| Diseases | MSH6 |
| SADR | 2956 |
| HugeNav | 2956 |
| wikipedia | MSH6 |
| MSH6 | |
| gopubmed | MSH6 |
| EVS | MSH6 |
| HEFalMp | MSH6 |
| MyGene2 | MSH6 |
| 23andMe | MSH6 |
| UniProt | P52701 |
| Ensembl | ENSG00000116062 |
| OMIM | 600678 |
| # SNPs | 424 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| i5037828 | |||
| i5037835 | |||
| i5037850 | |||
| i5037852 | |||
| i5037854 | |||
| i5037857 | |||
| i5037858 | |||
| i5037859 | |||
| i5037863 | |||
| i5037864 | |||
| i5037866 | |||
| i5037872 | |||
| i5037874 | |||
| i5037877 | |||
| i5037879 | |||
| i5037880 | |||
| i5037884 | |||
| i5037885 | |||
| i5037888 | |||
| i5037890 | |||
| i5037891 | |||
| i5037895 | |||
| i5046060 | |||
| i5046092 | |||
| i5046093 | |||
| i5046109 | |||
| i5046129 | |||
| i5046132 | |||
| i5900868 | |||
| i5900926 | |||
| i5900962 | |||
| i5901028 | |||
| i5901102 | |||
| i5901124 | |||
| i6015131 | |||
| i723181 | |||
| rs1042821 | 0 | 47,783,349 | |
| rs1057517551 | 0 | 47,798,891 | |
| rs1057517552 | 0 | 47,803,462 | |
| rs1057517763 | 0 | 47,804,920 | |
| rs1057517764 | 0 | 47,805,634 | |
| rs1057520605 | 0 | 47,798,839 | |
| rs1057524912 | 0 | 47,791,068 | |
| rs1060502875 | 0 | 47,791,108 | |
| rs1060502876 | 0 | 47,800,718 | |
| rs1060502881 | 0 | 47,805,638 | |
| rs1060502882 | 0 | 47,801,132 | |
| rs1060502886 | 0 | 47,799,798 | |
| rs1060502888 | 0 | 47,798,856 | |
| rs1060502890 | 0 | 47,800,974 | |
| ... further results | |||
MSH6 or mutS homolog 6 is a gene that codes for DNA mismatch repair protein Msh6 in the budding yeast Saccharomyces cerevisiae. It is the homologue of the human "G/T binding protein," (GTBP) also called p160 or hMSH6 (human MSH6). The MSH6 protein is a member of the Mutator S (MutS) family of proteins that are involved in DNA damage repair. Defects in hMSH6 are associated with atypical hereditary nonpolyposis colorectal cancer (Lynch syndrome)not fulfilling the Amsterdam criteria for HNPCC. hMSH6 mutations have also been linked to endometrial cancer and the development of endometrial carcinomas.Wikipedia
