SIK2
salt inducible kinase 2
Summary
Enables ATP binding activity; magnesium ion binding activity; and protein kinase activity. Involved in intracellular signal transduction and protein autophosphorylation. Is active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs542831 | 11:111,471,392 | T/A | upstream gene variant | — |
| rs1941598239 | 11:111,473,327 | C/G | — | uncertain significance |
| rs2135824810 | 11:111,473,348 | G/A | — | uncertain significance |
| rs2497852602 | 11:111,473,415 | A/G | — | uncertain significance |
| rs539524 | 11:111,477,325 | A/G | intron variant | — |
| rs570482879 | 11:111,505,264 | T/G | — | — |
| rs45487899 | 11:111,521,003 | C/T | intron variant | — |
| rs11608122 | 11:111,535,105 | C/T | intron variant | — |
| rs4459340 | 11:111,535,313 | G/C | — | — |
| rs9734135 | 11:111,536,190 | G/A | intron variant | — |
| rs746757174 | 11:111,572,231 | C/T | — | uncertain significance |
| rs201844240 | 11:111,573,941 | A/G | — | uncertain significance |
| rs367832665 | 11:111,574,035 | G/A | — | uncertain significance |
| rs778349552 | 11:111,582,995 | G/T | — | uncertain significance |
| rs151173495 | 11:111,583,026 | C/A | — | uncertain significance |
| rs200358202 | 11:111,583,073 | G/A | — | uncertain significance |
| rs2498224785 | 11:111,590,506 | G/T | — | uncertain significance |
| rs1424799440 | 11:111,590,700 | A/G | — | uncertain significance |
| rs1351307924 | 11:111,591,348 | A/G | — | uncertain significance |
| rs17113207 | 11:111,591,642 | A/G | — | benign |
| rs377735351 | 11:111,591,719 | C/T | — | uncertain significance |
| rs762577950 | 11:111,591,720 | G/A | — | likely benign |
| rs770510311 | 11:111,591,721 | G/C | — | uncertain significance |
| rs148331121 | 11:111,591,746 | C/T | — | uncertain significance |
| rs372467311 | 11:111,592,567 | A/G | — | uncertain significance |
| rs1366924913 | 11:111,592,624 | G/A | — | uncertain significance |
| rs1159792339 | 11:111,593,393 | C/T | — | uncertain significance |
| rs748015077 | 11:111,593,447 | C/T | — | uncertain significance |
| rs570457726 | 11:111,594,234 | G/A | — | uncertain significance |
| rs1003816615 | 11:111,594,329 | C/T | — | uncertain significance |
| rs144562229 | 11:111,594,336 | G/A | — | likely benign |
| rs201581603 | 11:111,594,372 | C/T | — | uncertain significance |
| rs1010619779 | 11:111,594,387 | A/T | — | uncertain significance |
| rs778917625 | 11:111,594,419 | G/A | — | uncertain significance |
| rs568139966 | 11:111,594,447 | G/A | — | uncertain significance |
| rs377257252 | 11:111,594,506 | C/G | — | uncertain significance |
| rs1565399445 | 11:111,594,516 | C/T | — | uncertain significance |
| rs147750033 | 11:111,594,551 | C/A | — | uncertain significance |
| rs45586732 | 11:111,594,557 | C/A | — | uncertain significance |
| rs768393488 | 11:111,594,632 | G/A | — | uncertain significance |
| rs2498264147 | 11:111,594,647 | C/G | — | uncertain significance |
| rs767803933 | 11:111,594,662 | C/A | — | uncertain significance |
| rs202037562 | 11:111,594,665 | T/G | — | uncertain significance |
| rs769532950 | 11:111,594,694 | G/C | — | uncertain significance |
| rs111845343 | 11:111,594,758 | G/A | — | uncertain significance |
| rs1242174079 | 11:111,594,815 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.