DGKQ
diacylglycerol kinase theta
Summary
The protein encoded by this gene contains three cysteine-rich domains, a proline-rich region, and a pleckstrin homology domain with an overlapping Ras-associating domain. It is localized in the speckle domains of the nucleus, and mediates the regeneration of phosphatidylinositol (PI) from diacylglycerol in the PI-cycle during cell signal transduction. [provided by RefSeq, Jul 2008]
Known Variants113 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs755244449 | 4:954,455 | C/T | — | uncertain significance |
| rs756990762 | 4:954,893 | C/T | — | uncertain significance |
| rs760056995 | 4:954,927 | G/T | — | likely benign |
| rs1711852589 | 4:954,935 | A/G | — | uncertain significance |
| rs772631722 | 4:954,977 | C/T | — | uncertain significance |
| rs369222961 | 4:954,996 | C/T | — | likely benign |
| rs373760127 | 4:955,247 | C/G | — | likely benign |
| rs145042207 | 4:955,257 | T/C | — | uncertain significance |
| rs201971574 | 4:955,263 | C/T | — | benign |
| rs367834282 | 4:955,266 | C/T | — | uncertain significance |
| rs759369106 | 4:955,271 | G/A | — | uncertain significance |
| rs143203696 | 4:955,530 | C/T | — | likely benign |
| rs1432092927 | 4:955,534 | C/G | — | uncertain significance |
| rs374287553 | 4:955,567 | G/A | — | uncertain significance |
| rs756318334 | 4:955,572 | T/C | — | uncertain significance |
| rs1448736434 | 4:955,588 | G/T | — | uncertain significance |
| rs200926485 | 4:955,600 | C/T | — | uncertain significance |
| rs77865682 | 4:955,632 | G/A | — | benign |
| rs987350759 | 4:955,830 | G/A | — | uncertain significance |
| rs770122049 | 4:955,851 | T/C | — | uncertain significance |
| rs1380526612 | 4:956,231 | G/A | — | uncertain significance |
| rs528009075 | 4:956,245 | G/A | — | uncertain significance |
| rs11946829 | 4:956,247 | G/A | — | benign |
| rs568501834 | 4:956,310 | G/A | — | likely benign |
| rs754016909 | 4:956,312 | C/T | — | uncertain significance |
| rs201671964 | 4:956,368 | G/C | — | uncertain significance |
| rs140567391 | 4:956,377 | C/T | — | uncertain significance |
| rs374968373 | 4:956,668 | C/T | — | uncertain significance |
| rs2533913695 | 4:956,706 | A/G | — | uncertain significance |
| rs543716400 | 4:956,917 | C/A | — | likely benign |
| rs754687362 | 4:956,929 | G/A | — | likely benign |
| rs995625705 | 4:956,955 | C/T | — | uncertain significance |
| rs1463376038 | 4:956,970 | G/A | — | uncertain significance |
| rs780230155 | 4:956,976 | G/C | — | uncertain significance |
| rs138974295 | 4:957,017 | C/T | — | uncertain significance |
| rs1712025546 | 4:957,036 | C/T | — | uncertain significance |
| rs199789034 | 4:957,056 | C/G | — | uncertain significance |
| rs768145892 | 4:958,954 | G/A | — | likely benign |
| rs764189185 | 4:958,998 | C/T | — | uncertain significance |
| rs1180775609 | 4:958,999 | G/A | — | uncertain significance |
| rs375891086 | 4:959,005 | G/A | — | uncertain significance |
| rs779858615 | 4:959,028 | A/G | — | uncertain significance |
| rs575557821 | 4:959,041 | C/T | — | uncertain significance |
| rs1045821854 | 4:959,073 | A/G | — | uncertain significance |
| rs186280586 | 4:959,083 | C/T | — | likely benign |
| rs143673932 | 4:959,529 | C/T | intron variant | — |
| rs749879528 | 4:959,748 | C/G | — | uncertain significance |
| rs1486949806 | 4:959,769 | C/T | — | uncertain significance |
| rs373971638 | 4:959,771 | G/A | — | likely benign |
| rs765814870 | 4:959,805 | G/A | — | uncertain significance |
| rs1469502538 | 4:959,820 | C/T | — | uncertain significance |
| rs373324474 | 4:959,822 | C/G | — | uncertain significance |
| rs150003997 | 4:959,830 | C/T | — | likely benign |
| rs771516814 | 4:960,258 | C/T | — | uncertain significance |
| rs1353361274 | 4:960,279 | A/G | — | uncertain significance |
| rs11248059 | 4:960,331 | C/G | — | benign |
| rs138551311 | 4:960,578 | C/G | — | uncertain significance |
| rs4690196 | 4:960,713 | G/A | regulatory region variant | — |
| rs1167587922 | 4:960,753 | T/G | — | uncertain significance |
| rs756554134 | 4:960,793 | G/A | — | uncertain significance |
| rs373584237 | 4:960,820 | C/G | — | uncertain significance |
| rs200194170 | 4:960,826 | C/T | — | uncertain significance |
| rs772878954 | 4:960,832 | C/A | — | uncertain significance |
| rs762561319 | 4:960,835 | C/T | — | uncertain significance |
| rs781005950 | 4:960,968 | C/T | — | uncertain significance |
| rs2533937292 | 4:960,978 | A/T | — | uncertain significance |
| rs766440558 | 4:961,002 | A/G | — | uncertain significance |
| rs576225867 | 4:961,005 | C/T | — | uncertain significance |
| rs777711317 | 4:961,017 | C/A | — | uncertain significance |
| rs200155030 | 4:961,122 | G/T | — | likely benign |
| rs2533938471 | 4:961,139 | A/G | — | uncertain significance |
| rs375110375 | 4:961,143 | C/T | — | uncertain significance |
| rs529521985 | 4:961,354 | C/T | — | likely benign |
| rs779125252 | 4:961,363 | G/A | — | uncertain significance |
| rs150670009 | 4:961,371 | G/T | — | uncertain significance |
| rs748214311 | 4:961,391 | T/G | — | uncertain significance |
| rs139905393 | 4:961,421 | C/A | — | uncertain significance |
| rs767921398 | 4:961,518 | G/T | — | uncertain significance |
| rs745672943 | 4:961,546 | C/A | — | uncertain significance |
| rs973933278 | 4:961,555 | C/A | — | uncertain significance |
| rs759837865 | 4:961,585 | C/T | — | uncertain significance |
| rs772371335 | 4:961,670 | G/A | — | uncertain significance |
| rs936982279 | 4:961,719 | C/T | — | uncertain significance |
| rs1277604283 | 4:961,727 | A/G | — | uncertain significance |
| rs758629181 | 4:961,739 | G/A | — | uncertain significance |
| rs113007498 | 4:961,760 | C/T | — | likely benign |
| rs1359568603 | 4:961,770 | C/T | — | uncertain significance |
| rs936504965 | 4:961,782 | C/T | — | uncertain significance |
| rs534332507 | 4:961,796 | G/A | — | uncertain significance |
| rs1350658406 | 4:962,074 | A/G | — | uncertain significance |
| rs1470511834 | 4:962,096 | C/T | — | uncertain significance |
| rs76581432 | 4:962,100 | G/A | — | benign |
| rs190556735 | 4:962,124 | C/G | — | likely benign |
| rs201406137 | 4:962,141 | C/G | — | uncertain significance |
| rs768749690 | 4:962,155 | G/A | — | uncertain significance |
| rs778262598 | 4:962,167 | C/G | — | uncertain significance |
| rs779782048 | 4:962,178 | G/C | — | uncertain significance |
| rs773803693 | 4:962,205 | G/A | — | likely benign |
| rs779325711 | 4:962,298 | C/A | — | uncertain significance |
| rs563757088 | 4:962,299 | G/A | — | uncertain significance |
Showing 100 of 113 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.