MTUS2
microtubule associated scaffold protein 2
Summary
Enables microtubule binding activity and protein homodimerization activity. Located in centrosome; cytoplasmic microtubule; and intercellular bridge. Part of nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1161463 | 13:29,431,338 | A/G | intergenic variant | — |
| rs327127 | 13:29,518,900 | C/G | intergenic variant | — |
| rs2758215 | 13:29,537,036 | G/C | intergenic variant | — |
| rs1331055288 | 13:29,599,394 | G/A | — | uncertain significance |
| rs1886497603 | 13:29,599,767 | A/T | — | uncertain significance |
| rs182740 | 13:29,599,829 | C/T | — | benign |
| rs375769908 | 13:29,600,007 | C/T | — | uncertain significance |
| rs183738371 | 13:29,600,055 | A/T | — | benign |
| rs200464295 | 13:29,600,272 | C/G | — | uncertain significance |
| rs199993580 | 13:29,600,340 | T/A | — | uncertain significance |
| rs775175224 | 13:29,600,597 | C/T | — | uncertain significance |
| rs200101021 | 13:29,600,630 | A/C | — | uncertain significance |
| rs2542341661 | 13:29,600,655 | A/G | — | uncertain significance |
| rs185213186 | 13:29,601,016 | A/C | — | uncertain significance |
| rs2479768 | 13:29,620,654 | A/C | — | — |
| rs61999321 | 13:29,898,783 | C/T | missense variant | — |
| rs369916182 | 13:29,933,425 | G/C | — | likely benign |
| rs112264341 | 13:29,933,583 | C/T | — | benign |
| rs2388082 | 13:29,961,332 | C/T | — | — |
| rs3125719 | 13:29,990,966 | T/A | — | — |
| rs144118917 | 13:30,054,307 | G/A | — | uncertain significance |
| rs749360854 | 13:30,054,317 | A/G | — | uncertain significance |
| rs756769441 | 13:30,054,344 | G/T | — | uncertain significance |
| rs1396125954 | 13:30,054,348 | C/T | — | likely benign |
| rs371828380 | 13:30,054,443 | G/A | — | uncertain significance |
| rs763654729 | 13:30,054,482 | G/A | — | uncertain significance |
| rs372511573 | 13:30,062,052 | G/A | — | uncertain significance |
| rs1329463819 | 13:30,062,111 | C/G | — | uncertain significance |
| rs2502635209 | 13:30,062,112 | C/G | — | uncertain significance |
| rs185151498 | 13:30,062,127 | G/A | — | uncertain significance |
| rs1882270103 | 13:30,066,788 | A/T | — | uncertain significance |
| rs1197516447 | 13:30,071,377 | C/G | — | uncertain significance |
| rs749901649 | 13:30,071,415 | G/A | — | uncertain significance |
| rs760822363 | 13:30,071,434 | C/G | — | uncertain significance |
| rs536439350 | 13:30,071,461 | G/T | — | uncertain significance |
| rs371216693 | 13:30,072,639 | G/A | — | uncertain significance |
| rs1448938499 | 13:30,075,270 | G/A | — | uncertain significance |
| rs767342697 | 13:30,077,204 | G/A | — | uncertain significance |
| rs7986532 | 13:30,077,217 | G/A | — | benign |
| rs189670967 | 13:30,077,272 | A/T | — | uncertain significance |
| rs766327837 | 13:30,077,288 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.