BRSK1
BR serine/threonine kinase 1
Summary
Enables magnesium ion binding activity and protein serine/threonine kinase activity. Involved in mitotic G2 DNA damage checkpoint signaling and protein phosphorylation. Acts upstream of or within G2/M transition of mitotic cell cycle; peptidyl-serine phosphorylation; and response to UV. Located in cell junction; cytoplasm; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747897862 | 19:55,798,401 | A/G | — | uncertain significance |
| rs12611091 | 19:55,800,329 | T/C | intron variant | — |
| rs200073194 | 19:55,800,916 | C/T | — | uncertain significance |
| rs2516356898 | 19:55,800,951 | G/T | — | uncertain significance |
| rs745487860 | 19:55,814,177 | G/A | — | uncertain significance |
| rs1470828063 | 19:55,814,682 | G/C | — | uncertain significance |
| rs17851414 | 19:55,815,072 | C/T | — | benign |
| rs753486933 | 19:55,815,073 | C/T | — | uncertain significance |
| rs1461425914 | 19:55,815,079 | G/A | — | uncertain significance |
| rs780991388 | 19:55,815,091 | C/T | — | uncertain significance |
| rs776766095 | 19:55,815,127 | G/C | — | uncertain significance |
| rs1241973397 | 19:55,815,163 | C/T | — | uncertain significance |
| rs536618174 | 19:55,815,164 | G/A | — | uncertain significance |
| rs190954611 | 19:55,815,952 | G/T | — | uncertain significance |
| rs1015322634 | 19:55,816,063 | C/A | — | uncertain significance |
| rs751823280 | 19:55,816,201 | G/A | — | uncertain significance |
| rs1163205688 | 19:55,816,210 | G/A | — | uncertain significance |
| rs1184412976 | 19:55,816,232 | A/G | — | uncertain significance |
| rs755640966 | 19:55,816,694 | A/G | — | uncertain significance |
| rs2088637068 | 19:55,816,886 | A/C | — | uncertain significance |
| rs201185885 | 19:55,816,895 | G/A | — | uncertain significance |
| rs141379955 | 19:55,817,644 | C/G | — | uncertain significance |
| rs370734031 | 19:55,817,686 | G/A | — | uncertain significance |
| rs754028790 | 19:55,817,759 | C/T | — | uncertain significance |
| rs200690719 | 19:55,817,765 | G/A | — | uncertain significance |
| rs79723785 | 19:55,818,225 | T/C | intron variant | — |
| rs1172822 | 19:55,819,845 | C/T | downstream gene variant | — |
| rs377342100 | 19:55,820,025 | A/G | — | uncertain significance |
| rs2516389505 | 19:55,820,073 | A/G | — | uncertain significance |
| rs763805486 | 19:55,823,324 | G/A | — | uncertain significance |
| rs370352134 | 19:55,823,348 | G/A | — | uncertain significance |
| rs761104183 | 19:55,823,378 | G/A | — | uncertain significance |
| rs7246479 | 19:55,824,332 | T/C | synonymous variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.