EML3
EMAP like 3
Summary
Predicted to enable microtubule binding activity. Involved in mitotic metaphase chromosome alignment and regulation of mitotic spindle assembly. Located in several cellular components, including midbody; mitotic spindle microtubule; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1389449961 | 11:62,369,993 | G/A | — | uncertain significance |
| rs757062449 | 11:62,370,091 | G/C | — | uncertain significance |
| rs774505119 | 11:62,370,137 | A/C | — | uncertain significance |
| rs1942308122 | 11:62,370,307 | T/C | — | uncertain significance |
| rs757439722 | 11:62,370,714 | C/T | — | uncertain significance |
| rs2496050472 | 11:62,371,492 | C/A | — | uncertain significance |
| rs2496050537 | 11:62,371,493 | C/A | — | uncertain significance |
| rs765670499 | 11:62,371,506 | C/A | — | uncertain significance |
| rs374273810 | 11:62,373,125 | T/G | — | uncertain significance |
| rs375303962 | 11:62,373,173 | G/A | — | uncertain significance |
| rs765218426 | 11:62,373,208 | G/A | — | uncertain significance |
| rs201324536 | 11:62,373,422 | T/C | — | uncertain significance |
| rs369914709 | 11:62,373,430 | A/G | — | uncertain significance |
| rs1311258538 | 11:62,373,431 | C/T | — | uncertain significance |
| rs146863965 | 11:62,373,572 | T/C | — | uncertain significance |
| rs2496087519 | 11:62,373,581 | C/T | — | uncertain significance |
| rs2496104069 | 11:62,374,439 | C/T | — | uncertain significance |
| rs2496104570 | 11:62,374,457 | T/C | — | uncertain significance |
| rs143273389 | 11:62,374,528 | G/A | — | uncertain significance |
| rs2496121316 | 11:62,375,194 | C/T | — | uncertain significance |
| rs142782428 | 11:62,375,253 | C/T | — | uncertain significance |
| rs147444035 | 11:62,375,744 | C/A | — | uncertain significance |
| rs1421853156 | 11:62,376,027 | G/A | — | uncertain significance |
| rs554043030 | 11:62,376,045 | C/T | — | uncertain significance |
| rs1942650927 | 11:62,376,070 | C/T | — | uncertain significance |
| rs139448366 | 11:62,376,112 | C/T | — | uncertain significance |
| rs1355030498 | 11:62,376,491 | C/A | — | uncertain significance |
| rs774522482 | 11:62,376,510 | G/A | — | uncertain significance |
| rs754722668 | 11:62,376,860 | C/G | — | uncertain significance |
| rs373348539 | 11:62,376,865 | G/A | — | uncertain significance |
| rs537470976 | 11:62,377,153 | G/C | — | uncertain significance |
| rs201745494 | 11:62,377,167 | G/A | — | uncertain significance |
| rs543507884 | 11:62,378,385 | C/A | — | uncertain significance |
| rs142822475 | 11:62,378,394 | T/C | — | uncertain significance |
| rs140915975 | 11:62,378,430 | A/G | — | uncertain significance |
| rs547084388 | 11:62,378,605 | G/A | — | uncertain significance |
| rs12808829 | 11:62,378,660 | G/A | synonymous variant | — |
| rs895592341 | 11:62,378,682 | T/C | — | uncertain significance |
| rs773623280 | 11:62,378,695 | G/A | — | uncertain significance |
| rs764663880 | 11:62,378,709 | C/T | — | uncertain significance |
| rs199907407 | 11:62,378,910 | G/A | — | uncertain significance |
| rs1455333059 | 11:62,378,916 | G/C | — | uncertain significance |
| rs1044935148 | 11:62,378,925 | A/G | — | likely benign |
| rs1024222583 | 11:62,379,923 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.