KIF3A
kinesin family member 3A
Summary
Enables protein phosphatase binding activity; small GTPase binding activity; and spectrin binding activity. Involved in protein localization to cell junction and protein transport. Located in centriole; centrosome; and spindle microtubule. Part of kinesin II complex. Biomarker of silicosis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11242123 | 5:132,025,487 | A/G | coding sequence variant | — |
| rs4705962 | 5:132,028,858 | T/C | 3 prime UTR variant | — |
| rs17690965 | 5:132,030,667 | C/G | 3 prime UTR variant | — |
| rs17166194 | 5:132,032,022 | C/T | 3 prime UTR variant | — |
| rs143233559 | 5:132,032,369 | C/T | — | uncertain significance |
| rs10455052 | 5:132,034,588 | C/A | intron variant | — |
| rs1178650333 | 5:132,036,389 | T/C | — | uncertain significance |
| rs201423876 | 5:132,037,789 | C/T | — | likely benign |
| rs1425389092 | 5:132,037,835 | G/A | — | uncertain significance |
| rs142021437 | 5:132,038,659 | T/G | — | uncertain significance |
| rs759731870 | 5:132,038,732 | T/C | — | uncertain significance |
| rs774233686 | 5:132,038,734 | T/C | — | uncertain significance |
| rs374997234 | 5:132,038,765 | T/A | — | likely benign |
| rs760704313 | 5:132,039,176 | T/A | — | uncertain significance |
| rs10062446 | 5:132,040,374 | T/A | intron variant | — |
| rs2299007 | 5:132,043,032 | A/G | intron variant | — |
| rs201305284 | 5:132,044,590 | A/G | — | likely benign |
| rs7737031 | 5:132,046,590 | C/T | intron variant | — |
| rs11740584 | 5:132,046,789 | G/A | intron variant | — |
| rs2897442 | 5:132,049,027 | C/A | — | — |
| rs2531912430 | 5:132,051,518 | C/A | — | uncertain significance |
| rs760913175 | 5:132,052,029 | C/T | — | uncertain significance |
| rs759314163 | 5:132,052,578 | T/A | — | uncertain significance |
| rs2531916980 | 5:132,052,609 | T/C | — | uncertain significance |
| rs2051809 | 5:132,056,874 | A/C | intron variant | — |
| rs143232016 | 5:132,061,834 | T/C | — | uncertain significance |
| rs1754323769 | 5:132,070,029 | T/C | — | uncertain significance |
| rs60168940 | 5:132,071,212 | C/T | intron variant | — |
| rs2277065 | 5:132,073,002 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.