| GENE NAME | MCM8 |
| CHROMOSOME | 20 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000125885 |
| UNIPROT ACCESSION NUMBER | Q9UJA3 |
| GO MOLECULAR FUNCTION | ['MutLbeta complex binding', 'chromatin binding', 'MutSalpha complex binding', 'single-stranded DNA binding', 'ATP hydrolysis activity', 'enzyme binding', 'ATP binding', 'single-stranded DNA helicase activity', 'MutSbeta complex binding', 'protein binding'] |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-113507; R-HSA-113510; R-HSA-1640170; R-HSA-176187; R-HSA-176974; R-HSA-453279; R-HSA-68689; R-HSA-68827; R-HSA-68867; R-HSA-68949; R-HSA-68962; R-HSA-69002; R-HSA-69052; R-HSA-69190; R-HSA-69206; R-HSA-69239; R-HSA-69242; R-HSA-69278; R-HSA-69306; R-HSA-69481; R-HSA-69620 |
| 1 combination linked to MCM8 | OLI1231 |
| 1 variant linked to MCM8 | MCM8:c.2132G>T, p.Gly671Val |
| 1 disease linked to MCM8 | Recurrent Pregnancy Loss |