STK35
serine/threonine kinase 35
Summary
The protein encoded by this gene is a kinase that is predominantly found in the nucleus. However, it can interact with PDLIM1/CLP-36 in the cytoplasm and localize to actin stress fibers. The encoded protein may be a regulator of actin stress fibers in nonmuscle cells. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768467924 | 20:2,082,588 | A/T | — | uncertain significance |
| rs528879204 | 20:2,082,628 | G/A | — | uncertain significance |
| rs770510417 | 20:2,082,703 | G/A | — | uncertain significance |
| rs914645476 | 20:2,082,707 | C/T | — | likely benign |
| rs929740729 | 20:2,082,714 | T/G | — | uncertain significance |
| rs2122531906 | 20:2,082,756 | G/C | — | uncertain significance |
| rs1253058103 | 20:2,082,762 | C/A | — | uncertain significance |
| rs980466082 | 20:2,083,429 | C/T | — | uncertain significance |
| rs2514428172 | 20:2,083,474 | G/A | — | uncertain significance |
| rs998130042 | 20:2,083,475 | G/C | — | uncertain significance |
| rs775775175 | 20:2,083,478 | C/T | — | uncertain significance |
| rs943195413 | 20:2,083,481 | G/C | — | uncertain significance |
| rs2514428252 | 20:2,083,511 | C/T | — | uncertain significance |
| rs756947580 | 20:2,083,528 | G/A | — | uncertain significance |
| rs745356612 | 20:2,083,553 | C/A | — | uncertain significance |
| rs1349405730 | 20:2,083,561 | C/T | — | uncertain significance |
| rs1985432085 | 20:2,083,598 | C/T | — | uncertain significance |
| rs2514428508 | 20:2,083,603 | A/G | — | likely benign |
| rs781004864 | 20:2,083,616 | C/T | — | uncertain significance |
| rs779313444 | 20:2,083,631 | G/A | — | likely benign |
| rs906109247 | 20:2,083,652 | C/T | — | uncertain significance |
| rs2514428713 | 20:2,083,673 | T/A | — | likely benign |
| rs1008549027 | 20:2,083,783 | G/A | — | uncertain significance |
| rs555115763 | 20:2,083,786 | C/G | — | uncertain significance |
| rs6137010 | 20:2,090,118 | C/T | intron variant | — |
| rs766616225 | 20:2,095,267 | G/C | — | — |
| rs1464306101 | 20:2,097,317 | A/G | — | uncertain significance |
| rs2514438434 | 20:2,097,623 | A/C | — | uncertain significance |
| rs6137042 | 20:2,100,095 | G/C | — | — |
| rs2096124 | 20:2,101,489 | G/T | — | — |
| rs6137103 | 20:2,121,249 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.