STK39
serine/threonine kinase 39
Summary
This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1061471 | 2:168,811,352 | C/T | 3 prime UTR variant | — |
| rs541206860 | 2:168,812,070 | C/T | — | uncertain significance |
| rs578031265 | 2:168,857,545 | C/T | — | — |
| rs6433027 | 2:168,864,360 | T/C | intron variant | — |
| rs201012106 | 2:168,920,059 | C/A | — | uncertain significance |
| rs1222091118 | 2:168,921,854 | T/G | — | uncertain significance |
| rs2468230025 | 2:168,986,109 | T/C | — | uncertain significance |
| rs2468259978 | 2:168,996,878 | G/A | — | uncertain significance |
| rs3754781 | 2:169,015,476 | G/A | intron variant | — |
| rs3754777 | 2:169,015,914 | C/G | — | — |
| rs3754775 | 2:169,016,263 | C/T | intron variant | — |
| rs200424635 | 2:169,020,307 | T/C | — | uncertain significance |
| rs200991167 | 2:169,020,322 | C/T | — | uncertain significance |
| rs376136352 | 2:169,020,354 | C/T | — | uncertain significance |
| rs4668039 | 2:169,025,379 | A/G | intron variant | — |
| rs80265589 | 2:169,027,979 | T/C | — | — |
| rs11892008 | 2:169,035,673 | C/T | intron variant | — |
| rs35929607 | 2:169,035,736 | A/T | — | — |
| rs6749447 | 2:169,041,386 | T/G | regulatory region variant | — |
| rs60587303 | 2:169,046,632 | T/C | regulatory region variant | — |
| rs2390669 | 2:169,091,942 | A/C | upstream gene variant | — |
| rs765358308 | 2:169,103,783 | C/T | — | uncertain significance |
| rs1240752153 | 2:169,103,786 | C/T | — | uncertain significance |
| rs1377642110 | 2:169,103,788 | G/A | — | uncertain significance |
| rs576855530 | 2:169,103,859 | C/G | — | likely benign |
| rs751683808 | 2:169,103,864 | G/C | — | uncertain significance |
| rs1690958418 | 2:169,103,867 | C/A | — | uncertain significance |
| rs767710354 | 2:169,103,884 | G/C | — | uncertain significance |
| rs748780606 | 2:169,103,910 | C/G | — | uncertain significance |
| rs747014948 | 2:169,103,930 | C/G | — | uncertain significance |
| rs76179989 | 2:169,103,999 | T/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.