MPHOSPH9
M-phase phosphoprotein 9
Summary
Involved in negative regulation of cilium assembly. Located in Golgi apparatus; centriole; and centrosome. Implicated in multiple sclerosis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61187102 | 12:123,639,869 | G/T | — | — |
| rs1727313 | 12:123,640,853 | C/T | — | — |
| rs766039097 | 12:123,641,374 | G/A | — | uncertain significance |
| rs752879448 | 12:123,641,400 | A/G | — | uncertain significance |
| rs1716162 | 12:123,642,538 | T/G | — | — |
| rs61041384 | 12:123,644,043 | T/C | intron variant | — |
| rs748163843 | 12:123,645,868 | C/T | — | uncertain significance |
| rs773346433 | 12:123,645,870 | G/A | — | likely benign |
| rs769035138 | 12:123,645,879 | C/A | — | uncertain significance |
| rs201364928 | 12:123,645,904 | C/A | — | uncertain significance |
| rs752545389 | 12:123,646,734 | C/T | — | uncertain significance |
| rs1186879944 | 12:123,646,740 | C/G | — | uncertain significance |
| rs1335995368 | 12:123,647,642 | T/C | — | uncertain significance |
| rs960422109 | 12:123,648,562 | C/T | — | uncertain significance |
| rs767780590 | 12:123,648,574 | T/C | — | uncertain significance |
| rs992217308 | 12:123,648,587 | T/C | — | uncertain significance |
| rs753978707 | 12:123,648,593 | G/C | — | uncertain significance |
| rs779304295 | 12:123,648,598 | C/T | — | uncertain significance |
| rs375735988 | 12:123,649,894 | A/G | — | uncertain significance |
| rs377560994 | 12:123,649,902 | C/T | — | likely benign |
| rs1366124917 | 12:123,651,277 | G/T | — | uncertain significance |
| rs2044337887 | 12:123,651,280 | T/C | — | uncertain significance |
| rs200560375 | 12:123,651,317 | C/T | — | uncertain significance |
| rs1716177 | 12:123,655,457 | C/A | — | — |
| rs1790100 | 12:123,656,725 | G/T | intron variant | — |
| rs967043661 | 12:123,657,619 | C/T | — | — |
| rs557051451 | 12:123,657,658 | A/G | — | — |
| rs1727310 | 12:123,660,510 | A/T | — | — |
| rs1727311 | 12:123,660,716 | T/G | intron variant | — |
| rs777110388 | 12:123,661,274 | C/T | — | uncertain significance |
| rs2851447 | 12:123,665,113 | G/A | — | — |
| rs997324930 | 12:123,665,750 | C/T | — | uncertain significance |
| rs2851436 | 12:123,667,354 | G/C | — | — |
| rs1790105 | 12:123,667,950 | T/G | — | — |
| rs1790135 | 12:123,669,235 | C/T | intron variant | — |
| rs1790086 | 12:123,672,518 | A/T | — | — |
| rs2102949 | 12:123,676,763 | G/A | intron variant | — |
| rs947875824 | 12:123,678,942 | C/T | — | uncertain significance |
| rs2045851661 | 12:123,678,965 | G/C | — | likely benign |
| rs149124520 | 12:123,679,039 | C/T | — | uncertain significance |
| rs200030647 | 12:123,679,072 | G/T | — | uncertain significance |
| rs749008721 | 12:123,679,090 | C/T | — | uncertain significance |
| rs2547465825 | 12:123,679,108 | G/T | — | uncertain significance |
| rs141974876 | 12:123,679,132 | C/T | — | uncertain significance |
| rs11614406 | 12:123,682,396 | C/T | intron variant | — |
| rs1452887543 | 12:123,682,795 | A/C | — | uncertain significance |
| rs374263250 | 12:123,682,840 | C/T | — | uncertain significance |
| rs2046256043 | 12:123,686,834 | C/T | — | uncertain significance |
| rs760096565 | 12:123,687,210 | A/C | — | uncertain significance |
| rs200496688 | 12:123,687,253 | G/T | — | uncertain significance |
| rs189088477 | 12:123,687,307 | C/A | — | uncertain significance |
| rs766630504 | 12:123,687,311 | G/C | — | uncertain significance |
| rs190649470 | 12:123,687,322 | T/C | — | uncertain significance |
| rs369646331 | 12:123,687,367 | C/T | — | uncertain significance |
| rs752802984 | 12:123,687,368 | G/T | — | uncertain significance |
| rs758357971 | 12:123,687,376 | A/G | — | uncertain significance |
| rs1247129612 | 12:123,687,403 | G/A | — | uncertain significance |
| rs372914507 | 12:123,687,414 | G/A | — | uncertain significance |
| rs2046283833 | 12:123,687,443 | T/G | — | uncertain significance |
| rs758323407 | 12:123,687,498 | G/C | — | uncertain significance |
| rs2547487417 | 12:123,687,514 | G/T | — | uncertain significance |
| rs147539988 | 12:123,687,517 | C/T | — | uncertain significance |
| rs2547487807 | 12:123,687,600 | T/C | — | uncertain significance |
| rs778780184 | 12:123,687,915 | G/C | — | uncertain significance |
| rs372336414 | 12:123,687,919 | T/C | — | uncertain significance |
| rs113804400 | 12:123,688,780 | C/T | intron variant | — |
| rs2851443 | 12:123,694,250 | C/G | — | — |
| rs181390489 | 12:123,694,622 | G/A | — | uncertain significance |
| rs746744788 | 12:123,694,677 | T/C | — | uncertain significance |
| rs11057195 | 12:123,697,972 | G/C | intron variant | — |
| rs1790132 | 12:123,698,519 | G/C | — | — |
| rs1727324 | 12:123,698,603 | A/G | — | — |
| rs2046889711 | 12:123,699,351 | C/G | — | uncertain significance |
| rs771509814 | 12:123,699,354 | G/A | — | uncertain significance |
| rs775145873 | 12:123,699,358 | A/C | — | uncertain significance |
| rs187857615 | 12:123,702,934 | G/C | — | uncertain significance |
| rs375096191 | 12:123,702,954 | T/C | — | likely benign |
| rs2695480 | 12:123,704,569 | C/A | — | — |
| rs372132815 | 12:123,706,043 | T/C | — | uncertain significance |
| rs375172540 | 12:123,706,093 | G/A | — | likely benign |
| rs779902952 | 12:123,706,142 | C/T | — | uncertain significance |
| rs772341975 | 12:123,706,183 | C/G | — | uncertain significance |
| rs10744149 | 12:123,708,490 | T/G | — | — |
| rs537199690 | 12:123,709,822 | C/A | — | — |
| rs2851435 | 12:123,712,416 | G/C | — | — |
| rs1716169 | 12:123,716,930 | A/G | — | — |
| rs7304782 | 12:123,719,444 | G/T | — | — |
| rs11057204 | 12:123,725,827 | T/A | — | — |
| rs7313483 | 12:123,726,834 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.