| GENE NAME | MSH5 |
| CHROMOSOME | 6 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000204410 |
| UNIPROT ACCESSION NUMBER | A0A140T982 |
| GO MOLECULAR FUNCTION | ['mismatched DNA binding', 'double-stranded DNA binding', 'protein binding', 'ATP binding'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | R-HSA-1474165; R-HSA-1500620; R-HSA-1640170; R-HSA-912446; R-HSA-1474165; R-HSA-1500620; R-HSA-1640170; R-HSA-912446; R-HSA-1474165; R-HSA-1500620; R-HSA-1640170; R-HSA-912446; R-HSA-1474165; R-HSA-1500620; R-HSA-1640170; R-HSA-912446; R-HSA-1474165; R-HSA-1500620; R-HSA-1640170; R-HSA-912446 |
| 2 combinations linked to MSH5 | OLI1730; OLI1723 |
| 2 variants linked to MSH5 | MSH5:c.826C>T, p.Arg276Cys; MSH5:c.1051C>G, p.Arg351Gly |
| 1 disease linked to MSH5 | Primary ovarian failure |