SRPK1
SRSF protein kinase 1
Summary
This gene encodes a serine/arginine protein kinase specific for the SR (serine/arginine-rich domain) family of splicing factors. The protein localizes to the nucleus and the cytoplasm. It is thought to play a role in regulation of both constitutive and alternative splicing by regulating intracellular localization of splicing factors. Alternative splicing of this gene results in multiple transcript variants. Additional alternatively spliced transcript variants have been described for this gene, but their full length nature have not been determined.[provided by RefSeq, Jul 2010]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12198487 | 6:35,801,020 | T/C | 3 prime UTR variant | — |
| rs2534470429 | 6:35,803,085 | G/A | — | uncertain significance |
| rs181923979 | 6:35,819,758 | T/C | intron variant | — |
| rs531579065 | 6:35,826,123 | A/T | — | — |
| rs752901350 | 6:35,836,861 | C/T | — | uncertain significance |
| rs748987695 | 6:35,837,270 | A/G | — | uncertain significance |
| rs768150388 | 6:35,837,277 | C/T | — | uncertain significance |
| rs376417169 | 6:35,837,429 | C/G | — | uncertain significance |
| rs1473934058 | 6:35,837,590 | A/C | — | uncertain significance |
| rs745845504 | 6:35,837,664 | T/C | — | uncertain significance |
| rs370292368 | 6:35,838,195 | C/T | — | uncertain significance |
| rs1304899644 | 6:35,840,451 | T/C | — | uncertain significance |
| rs375747918 | 6:35,840,469 | G/T | — | uncertain significance |
| rs7743898 | 6:35,849,938 | T/A | — | — |
| rs530168482 | 6:35,853,073 | C/G | — | — |
| rs1367058234 | 6:35,854,530 | T/C | — | uncertain significance |
| rs776427708 | 6:35,855,814 | C/T | — | uncertain significance |
| rs931805875 | 6:35,855,883 | T/C | — | uncertain significance |
| rs752404523 | 6:35,856,672 | A/C | — | uncertain significance |
| rs35519113 | 6:35,856,679 | A/G | — | uncertain significance |
| rs2395642 | 6:35,857,222 | C/T | intron variant | — |
| rs1205447415 | 6:35,858,677 | C/A | — | uncertain significance |
| rs374942695 | 6:35,858,684 | C/T | — | uncertain significance |
| rs750403444 | 6:35,858,689 | G/C | — | uncertain significance |
| rs146165391 | 6:35,867,001 | C/T | intron variant | — |
| rs111812001 | 6:35,873,567 | G/A | — | — |
| rs138817242 | 6:35,875,932 | T/C | intron variant | — |
| rs11752499 | 6:35,883,488 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.