KIF17
kinesin family member 17
Summary
Predicted to enable ATP hydrolysis activity; microtubule binding activity; and plus-end-directed microtubule motor activity. Predicted to be involved in anterograde dendritic transport of neurotransmitter receptor complex and cell projection organization. Predicted to act upstream of or within microtubule-based process; protein-containing complex localization; and vesicle-mediated transport. Predicted to be located in cytosol. Predicted to be part of kinesin complex. Predicted to be active in several cellular components, including cilium; microtubule cytoskeleton; and postsynapse. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants103 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2053493192 | 1:20,991,163 | G/A | — | uncertain significance |
| rs2545297876 | 1:20,991,217 | T/A | — | uncertain significance |
| rs376184055 | 1:20,991,243 | G/A | — | uncertain significance |
| rs1157001562 | 1:20,992,738 | C/A | — | uncertain significance |
| rs912829749 | 1:20,992,811 | T/A | — | uncertain significance |
| rs191366066 | 1:20,996,905 | G/A | — | likely benign |
| rs76364354 | 1:20,996,917 | G/A | — | benign |
| rs200150083 | 1:20,996,951 | C/T | — | uncertain significance |
| rs769607660 | 1:20,998,449 | T/G | — | uncertain significance |
| rs1233422608 | 1:20,998,470 | T/C | — | uncertain significance |
| rs577775020 | 1:20,998,611 | G/A | — | uncertain significance |
| rs149211267 | 1:20,998,685 | C/T | — | uncertain significance |
| rs112287566 | 1:20,999,300 | C/A | intron variant | — |
| rs145153675 | 1:21,009,183 | C/T | — | uncertain significance |
| rs115257742 | 1:21,009,189 | T/C | — | uncertain significance |
| rs139817126 | 1:21,009,211 | C/T | — | likely benign |
| rs756546397 | 1:21,009,229 | C/A | — | uncertain significance |
| rs200844482 | 1:21,009,232 | C/T | — | uncertain significance |
| rs148629128 | 1:21,009,279 | C/T | — | uncertain significance |
| rs151177164 | 1:21,009,280 | G/C | — | uncertain significance |
| rs139870251 | 1:21,009,294 | C/T | — | uncertain significance |
| rs374049433 | 1:21,009,303 | C/T | — | uncertain significance |
| rs770910500 | 1:21,009,325 | C/T | — | uncertain significance |
| rs531505555 | 1:21,009,355 | C/A | — | uncertain significance |
| rs547112275 | 1:21,009,383 | G/A | — | likely benign |
| rs2545398343 | 1:21,011,308 | A/G | — | uncertain significance |
| rs566583367 | 1:21,011,339 | G/C | — | uncertain significance |
| rs779989905 | 1:21,011,380 | C/T | — | uncertain significance |
| rs768471031 | 1:21,011,390 | C/G | — | uncertain significance |
| rs143758204 | 1:21,011,401 | G/A | — | likely benign |
| rs139742596 | 1:21,011,440 | T/G | — | uncertain significance |
| rs1198742909 | 1:21,011,443 | G/A | — | uncertain significance |
| rs1363587083 | 1:21,011,456 | C/A | — | uncertain significance |
| rs188255115 | 1:21,011,519 | T/C | — | benign |
| rs771591340 | 1:21,012,554 | G/T | — | uncertain significance |
| rs1228359913 | 1:21,012,574 | C/T | — | uncertain significance |
| rs137916833 | 1:21,012,595 | C/T | — | uncertain significance |
| rs187149276 | 1:21,012,613 | C/A | — | likely benign |
| rs35103949 | 1:21,013,719 | C/A | intron variant | — |
| rs1158816257 | 1:21,013,975 | G/A | — | uncertain significance |
| rs200690761 | 1:21,014,098 | C/G | — | uncertain significance |
| rs370414135 | 1:21,014,101 | C/T | — | uncertain significance |
| rs1422807383 | 1:21,014,119 | G/A | — | uncertain significance |
| rs528825687 | 1:21,014,156 | C/G | — | uncertain significance |
| rs762663001 | 1:21,014,162 | A/T | — | uncertain significance |
| rs766885886 | 1:21,014,168 | C/T | — | uncertain significance |
| rs367672816 | 1:21,014,186 | C/G | — | uncertain significance |
| rs2545414799 | 1:21,014,224 | G/C | — | uncertain significance |
| rs2545415161 | 1:21,014,285 | C/T | — | uncertain significance |
| rs768877673 | 1:21,014,311 | G/A | — | likely benign |
| rs200910771 | 1:21,014,335 | A/G | — | likely benign |
| rs1233633573 | 1:21,014,354 | C/G | — | uncertain significance |
| rs147249030 | 1:21,014,374 | C/G | — | likely benign |
| rs756582673 | 1:21,014,395 | A/G | — | uncertain significance |
| rs2545416033 | 1:21,014,419 | C/T | — | likely benign |
| rs2545426130 | 1:21,016,683 | G/A | — | uncertain significance |
| rs112930242 | 1:21,016,688 | C/G | — | uncertain significance |
| rs746302711 | 1:21,016,693 | G/A | — | uncertain significance |
| rs140125368 | 1:21,016,737 | C/T | — | uncertain significance |
| rs1570455916 | 1:21,016,743 | G/A | — | uncertain significance |
| rs2545427007 | 1:21,016,804 | G/C | — | uncertain significance |
| rs373523975 | 1:21,024,876 | C/T | — | uncertain significance |
| rs748057322 | 1:21,024,964 | C/A | — | uncertain significance |
| rs2545481275 | 1:21,030,957 | C/T | — | uncertain significance |
| rs749266864 | 1:21,030,966 | T/C | — | uncertain significance |
| rs368449465 | 1:21,030,974 | G/C | — | uncertain significance |
| rs757201811 | 1:21,031,039 | T/G | — | uncertain significance |
| rs528572676 | 1:21,031,119 | G/A | — | uncertain significance |
| rs142534674 | 1:21,031,159 | C/T | — | uncertain significance |
| rs776259696 | 1:21,031,182 | C/T | — | uncertain significance |
| rs777648602 | 1:21,031,210 | C/T | — | likely benign |
| rs1214369075 | 1:21,031,254 | A/G | — | uncertain significance |
| rs200488493 | 1:21,031,276 | T/C | — | uncertain significance |
| rs765233832 | 1:21,031,327 | G/A | — | uncertain significance |
| rs201696480 | 1:21,031,386 | C/T | — | uncertain significance |
| rs6702859 | 1:21,031,983 | A/G | intron variant | — |
| rs875015 | 1:21,033,639 | G/A | — | — |
| rs200568311 | 1:21,036,156 | T/C | — | uncertain significance |
| rs2054402980 | 1:21,036,177 | G/A | — | uncertain significance |
| rs775858871 | 1:21,036,200 | G/A | — | uncertain significance |
| rs369376665 | 1:21,036,207 | C/T | — | uncertain significance |
| rs754438385 | 1:21,036,216 | G/A | — | uncertain significance |
| rs1474258144 | 1:21,036,255 | C/T | — | uncertain significance |
| rs377444908 | 1:21,036,258 | C/T | — | uncertain significance |
| rs547253363 | 1:21,036,297 | C/T | — | uncertain significance |
| rs781431910 | 1:21,039,958 | G/C | — | uncertain significance |
| rs371219583 | 1:21,039,984 | C/T | — | uncertain significance |
| rs536519322 | 1:21,040,009 | G/T | — | uncertain significance |
| rs750363854 | 1:21,040,020 | C/T | — | uncertain significance |
| rs766334139 | 1:21,040,021 | G/A | — | uncertain significance |
| rs751773843 | 1:21,040,024 | C/T | — | uncertain significance |
| rs558662591 | 1:21,041,992 | G/C | — | uncertain significance |
| rs2154538032 | 1:21,042,015 | C/T | — | uncertain significance |
| rs150545264 | 1:21,042,043 | C/T | — | benign |
| rs758746393 | 1:21,042,044 | G/A | — | uncertain significance |
| rs143703360 | 1:21,042,117 | A/G | — | uncertain significance |
| rs779848495 | 1:21,044,000 | A/G | — | uncertain significance |
| rs748329683 | 1:21,044,016 | G/A | — | uncertain significance |
| rs149468609 | 1:21,044,052 | T/C | — | likely benign |
| rs764963538 | 1:21,044,061 | C/G | — | uncertain significance |
Showing 100 of 103 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.