KIF9
kinesin family member 9
Summary
Enables identical protein binding activity. Involved in extracellular matrix disassembly; organelle disassembly; and regulation of podosome assembly. Located in microtubule; podosome; and vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs780934048 | 3:47,270,192 | G/T | — | uncertain significance |
| rs550761144 | 3:47,275,341 | A/G | — | — |
| rs755885776 | 3:47,277,034 | A/G | — | uncertain significance |
| rs2545800314 | 3:47,277,534 | A/G | — | uncertain significance |
| rs560394239 | 3:47,277,561 | C/G | — | uncertain significance |
| rs777193969 | 3:47,277,595 | T/A | — | uncertain significance |
| rs1195325409 | 3:47,277,598 | C/G | — | uncertain significance |
| rs778271494 | 3:47,278,023 | G/A | — | uncertain significance |
| rs1183096045 | 3:47,278,053 | G/T | — | uncertain significance |
| rs146414099 | 3:47,281,233 | A/T | coding sequence variant | — |
| rs539846029 | 3:47,281,780 | G/A | — | — |
| rs2545830498 | 3:47,282,305 | A/G | — | uncertain significance |
| rs762363234 | 3:47,282,310 | C/A | — | uncertain significance |
| rs200005957 | 3:47,282,313 | C/G | — | uncertain significance |
| rs780918981 | 3:47,282,350 | C/T | — | uncertain significance |
| rs147260286 | 3:47,282,362 | T/C | — | uncertain significance |
| rs2545831185 | 3:47,282,391 | T/A | — | uncertain significance |
| rs1466153285 | 3:47,282,479 | A/G | — | uncertain significance |
| rs749219695 | 3:47,282,494 | G/A | — | uncertain significance |
| rs12495173 | 3:47,282,899 | C/T | intron variant | — |
| rs114109244 | 3:47,284,551 | G/A | — | uncertain significance |
| rs142319729 | 3:47,284,611 | G/A | — | uncertain significance |
| rs369153866 | 3:47,286,293 | T/C | — | uncertain significance |
| rs565844112 | 3:47,286,297 | A/G | — | uncertain significance |
| rs200213936 | 3:47,287,700 | G/A | — | uncertain significance |
| rs142546493 | 3:47,287,709 | T/A | — | uncertain significance |
| rs765678929 | 3:47,287,710 | G/C | — | uncertain significance |
| rs201223058 | 3:47,288,867 | A/T | — | uncertain significance |
| rs372157611 | 3:47,288,923 | C/G | — | uncertain significance |
| rs372976130 | 3:47,289,519 | G/T | — | uncertain significance |
| rs760196363 | 3:47,289,525 | C/T | — | uncertain significance |
| rs559408366 | 3:47,291,609 | T/A | — | — |
| rs13065991 | 3:47,298,234 | A/G | regulatory region variant | — |
| rs2545965706 | 3:47,305,793 | C/T | — | uncertain significance |
| rs1701161011 | 3:47,305,807 | A/G | — | uncertain significance |
| rs138701088 | 3:47,307,226 | A/T | — | uncertain significance |
| rs778295274 | 3:47,307,301 | T/C | — | uncertain significance |
| rs1285035151 | 3:47,308,734 | A/G | — | uncertain significance |
| rs7636423 | 3:47,309,134 | C/G | intron variant | — |
| rs58472056 | 3:47,311,154 | T/A | — | — |
| rs1701637183 | 3:47,312,869 | A/T | — | uncertain significance |
| rs756391327 | 3:47,312,876 | T/C | — | uncertain significance |
| rs777042671 | 3:47,315,055 | C/T | — | uncertain significance |
| rs2546017218 | 3:47,315,068 | C/T | — | uncertain significance |
| rs780831766 | 3:47,316,875 | C/T | — | uncertain significance |
| rs148184082 | 3:47,316,925 | T/C | — | uncertain significance |
| rs2546025207 | 3:47,316,937 | A/C | — | uncertain significance |
| rs375774821 | 3:47,318,787 | G/A | — | likely benign |
| rs76198671 | 3:47,318,830 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.