NEK6
NIMA related kinase 6
Summary
The protein encoded by this gene is a kinase required for progression through the metaphase portion of mitosis. Inhibition of the encoded protein can lead to apoptosis. This protein also can enhance tumorigenesis by suppressing tumor cell senescence. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2026190 | 9:127,023,263 | G/C | — | — |
| rs34011920 | 9:127,027,412 | C/T | regulatory region variant | — |
| rs12379417 | 9:127,029,736 | G/T | — | — |
| rs4838147 | 9:127,034,352 | A/G | intron variant | — |
| rs35956754 | 9:127,034,358 | G/C | intron variant | — |
| rs760001393 | 9:127,055,241 | T/A | — | uncertain significance |
| rs753103515 | 9:127,055,290 | G/T | — | uncertain significance |
| rs768065021 | 9:127,064,218 | G/A | — | uncertain significance |
| rs377403028 | 9:127,064,272 | A/G | — | uncertain significance |
| rs2538283701 | 9:127,064,280 | A/T | — | uncertain significance |
| rs2538283717 | 9:127,064,283 | T/C | — | likely benign |
| rs145488745 | 9:127,064,291 | C/A | — | uncertain significance |
| rs867678055 | 9:127,064,307 | G/T | — | uncertain significance |
| rs3758212 | 9:127,069,753 | C/T | intron variant | — |
| rs769243779 | 9:127,074,800 | A/G | — | likely benign |
| rs774694008 | 9:127,074,801 | C/T | — | uncertain significance |
| rs148262318 | 9:127,074,839 | G/A | — | uncertain significance |
| rs150614386 | 9:127,076,240 | T/C | — | benign |
| rs771234776 | 9:127,076,252 | C/G | — | uncertain significance |
| rs2538378068 | 9:127,083,845 | C/G | — | uncertain significance |
| rs10818943 | 9:127,087,740 | C/T | regulatory region variant | — |
| rs368466543 | 9:127,088,637 | C/T | — | uncertain significance |
| rs751958560 | 9:127,088,681 | G/A | — | uncertain significance |
| rs369950028 | 9:127,088,699 | C/T | — | uncertain significance |
| rs3780204 | 9:127,092,887 | C/T | — | — |
| rs10986320 | 9:127,093,902 | C/G | regulatory region variant | — |
| rs1024255 | 9:127,094,481 | G/A | intron variant | — |
| rs779050538 | 9:127,101,921 | T/G | — | uncertain significance |
| rs151138282 | 9:127,110,026 | G/A | — | uncertain significance |
| rs779084313 | 9:127,110,081 | G/A | — | uncertain significance |
| rs144052872 | 9:127,110,096 | G/A | — | uncertain significance |
| rs200235098 | 9:127,113,179 | G/A | — | uncertain significance |
| rs1414669747 | 9:127,113,204 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.