STK33
serine/threonine kinase 33
Summary
Enables protein serine/threonine kinase activity. Involved in spermatogenesis. Predicted to be located in manchette. Predicted to be active in nucleus. Implicated in colorectal cancer; depressive disorder; and spermatogenic failure 93. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751336523 | 11:8,414,076 | C/G | — | uncertain significance |
| rs373984158 | 11:8,414,086 | C/T | — | uncertain significance |
| rs762420940 | 11:8,414,139 | G/T | — | uncertain significance |
| rs776825659 | 11:8,414,194 | T/C | — | uncertain significance |
| rs1467592777 | 11:8,414,204 | C/G | — | uncertain significance |
| rs779550632 | 11:8,414,214 | T/C | — | uncertain significance |
| rs73402082 | 11:8,427,377 | T/G | intron variant | — |
| rs1564891883 | 11:8,435,080 | C/G | — | uncertain significance |
| rs140349792 | 11:8,435,100 | T/G | — | conflicting classifications of pathogenicity |
| rs145552076 | 11:8,435,130 | G/C | — | uncertain significance |
| rs2541249613 | 11:8,435,148 | G/A | — | uncertain significance |
| rs763109430 | 11:8,435,157 | T/C | — | uncertain significance |
| rs1390881906 | 11:8,435,163 | A/T | — | likely benign |
| rs774490392 | 11:8,435,175 | T/C | — | uncertain significance |
| rs199562993 | 11:8,457,082 | T/C | — | uncertain significance |
| rs2547913803 | 11:8,457,091 | G/C | — | uncertain significance |
| rs1057520013 | 11:8,457,665 | A/C | missense variant | — |
| rs2547923763 | 11:8,457,672 | G/A | — | uncertain significance |
| rs936275480 | 11:8,462,238 | C/T | — | likely benign |
| rs914896685 | 11:8,462,275 | G/C | — | uncertain significance |
| rs1946449173 | 11:8,474,436 | T/G | — | uncertain significance |
| rs769131449 | 11:8,476,293 | T/G | — | uncertain significance |
| rs762840417 | 11:8,476,325 | A/G | — | likely benign |
| rs577298626 | 11:8,476,335 | T/C | — | uncertain significance |
| rs1003337576 | 11:8,476,359 | T/G | — | uncertain significance |
| rs537936728 | 11:8,478,918 | C/T | — | uncertain significance |
| rs141539888 | 11:8,478,968 | C/T | — | uncertain significance |
| rs371394045 | 11:8,478,983 | T/C | — | uncertain significance |
| rs2548187760 | 11:8,478,990 | C/G | — | uncertain significance |
| rs369943323 | 11:8,483,384 | T/C | — | uncertain significance |
| rs10769908 | 11:8,484,089 | C/T | intron variant | — |
| rs377716389 | 11:8,486,294 | C/T | — | uncertain significance |
| rs763906449 | 11:8,486,366 | T/C | — | uncertain significance |
| rs1948945011 | 11:8,494,729 | T/C | — | uncertain significance |
| rs34525052 | 11:8,494,755 | T/G | missense variant | — |
| rs201709884 | 11:8,494,771 | C/T | — | uncertain significance |
| rs771875782 | 11:8,494,772 | G/A | — | uncertain significance |
| rs1013006184 | 11:8,494,779 | T/C | — | likely benign |
| rs2548372120 | 11:8,496,263 | T/C | — | uncertain significance |
| rs144113279 | 11:8,496,305 | T/C | — | uncertain significance |
| rs368557393 | 11:8,496,311 | T/C | — | uncertain significance |
| rs7945659 | 11:8,529,925 | A/C | — | — |
| rs67257872 | 11:8,530,218 | A/C | — | — |
| rs377505014 | 11:8,578,795 | G/T | — | — |
| rs4929949 | 11:8,604,593 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.