KIF25
kinesin family member 25
Summary
The protein encoded by this gene is a member of the kinesin-like protein family. Protein family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. However, the particular function of this gene product has not yet been determined. Two alternatively spliced transcript variants which encode products have been described. Other splice variants have been found that lack exon 2 and the initiation codon for translation. [provided by RefSeq, Jul 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146495006 | 6:168,431,473 | C/T | — | uncertain significance |
| rs34049091 | 6:168,431,481 | G/A | — | benign |
| rs34981094 | 6:168,431,498 | G/A | — | likely benign |
| rs1554251035 | 6:168,431,500 | G/A | — | uncertain significance |
| rs754299875 | 6:168,431,511 | A/T | — | uncertain significance |
| rs2257743 | 6:168,431,687 | G/A | regulatory region variant | — |
| rs2539479700 | 6:168,434,580 | G/A | — | uncertain significance |
| rs1798978014 | 6:168,434,603 | G/A | — | uncertain significance |
| rs776435400 | 6:168,434,617 | A/G | — | uncertain significance |
| rs140045881 | 6:168,434,633 | C/T | — | uncertain significance |
| rs780114962 | 6:168,434,654 | C/T | — | uncertain significance |
| rs980690597 | 6:168,434,681 | T/G | — | uncertain significance |
| rs528450789 | 6:168,434,684 | T/C | — | uncertain significance |
| rs2539480040 | 6:168,434,689 | A/G | — | uncertain significance |
| rs146732504 | 6:168,434,704 | C/A | missense variant | — |
| rs757087872 | 6:168,439,252 | T/C | — | uncertain significance |
| rs1046586766 | 6:168,439,289 | T/C | — | uncertain significance |
| rs199605266 | 6:168,439,333 | G/T | — | uncertain significance |
| rs199500143 | 6:168,439,363 | G/C | — | uncertain significance |
| rs533395739 | 6:168,440,752 | G/C | — | uncertain significance |
| rs762420155 | 6:168,440,758 | G/A | — | uncertain significance |
| rs376174983 | 6:168,440,770 | A/T | — | uncertain significance |
| rs556267996 | 6:168,440,778 | C/T | — | likely benign |
| rs2539492272 | 6:168,440,815 | A/G | — | uncertain significance |
| rs2114912834 | 6:168,440,841 | G/C | — | uncertain significance |
| rs757536915 | 6:168,442,660 | T/C | — | uncertain significance |
| rs1482842754 | 6:168,442,773 | T/G | — | uncertain significance |
| rs752520655 | 6:168,442,823 | A/G | — | uncertain significance |
| rs774856116 | 6:168,443,291 | C/T | — | uncertain significance |
| rs773210209 | 6:168,443,296 | C/A | — | uncertain significance |
| rs1446881065 | 6:168,443,298 | T/C | — | uncertain significance |
| rs146787013 | 6:168,443,315 | G/A | — | benign |
| rs55745352 | 6:168,443,403 | G/A | — | benign |
| rs752334712 | 6:168,445,528 | T/C | — | uncertain significance |
| rs148150081 | 6:168,445,583 | G/A | — | likely benign |
| rs774850626 | 6:168,445,597 | G/A | — | uncertain significance |
| rs199726799 | 6:168,445,615 | G/A | — | uncertain significance |
| rs533895723 | 6:168,445,636 | C/T | — | uncertain significance |
| rs761327564 | 6:168,445,669 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.