HIPK3
homeodomain interacting protein kinase 3
Summary
Enables protein serine/threonine kinase activity. Involved in mRNA transcription; negative regulation of apoptotic process; and protein phosphorylation. Located in cytosol; nuclear body; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs148530680 | 11:33,308,084 | C/T | missense variant | — |
| rs1312887666 | 11:33,308,088 | C/T | — | uncertain significance |
| rs1367121509 | 11:33,308,132 | A/G | — | uncertain significance |
| rs2494779398 | 11:33,308,171 | C/T | — | uncertain significance |
| rs563248984 | 11:33,308,175 | G/A | — | uncertain significance |
| rs1851564125 | 11:33,308,243 | A/G | — | uncertain significance |
| rs375017758 | 11:33,308,292 | C/T | — | uncertain significance |
| rs187022690 | 11:33,308,298 | G/A | — | uncertain significance |
| rs368850984 | 11:33,308,331 | G/A | — | uncertain significance |
| rs777509665 | 11:33,308,727 | A/G | — | uncertain significance |
| rs938522132 | 11:33,308,904 | G/C | — | uncertain significance |
| rs142299107 | 11:33,308,963 | C/T | — | uncertain significance |
| rs2494784252 | 11:33,309,044 | T/C | — | uncertain significance |
| rs16924133 | 11:33,325,376 | A/T | intron variant | — |
| rs144565971 | 11:33,358,684 | T/A | — | uncertain significance |
| rs1565093611 | 11:33,360,380 | T/G | — | uncertain significance |
| rs266472 | 11:33,360,381 | G/A | — | benign |
| rs540576523 | 11:33,360,933 | T/C | — | uncertain significance |
| rs371957082 | 11:33,361,023 | C/T | — | uncertain significance |
| rs998774722 | 11:33,361,047 | T/C | — | uncertain significance |
| rs762484561 | 11:33,362,596 | C/T | — | uncertain significance |
| rs755886595 | 11:33,362,636 | C/T | — | uncertain significance |
| rs140757794 | 11:33,362,656 | G/A | — | uncertain significance |
| rs779133811 | 11:33,368,869 | G/A | — | uncertain significance |
| rs140297828 | 11:33,368,879 | A/G | — | uncertain significance |
| rs112993351 | 11:33,368,880 | A/T | — | uncertain significance |
| rs181305871 | 11:33,369,229 | C/T | — | uncertain significance |
| rs1009342386 | 11:33,369,292 | G/A | — | uncertain significance |
| rs55807239 | 11:33,369,439 | C/T | — | uncertain significance |
| rs1853546608 | 11:33,369,470 | A/T | — | uncertain significance |
| rs775773329 | 11:33,369,482 | G/T | — | uncertain significance |
| rs143841994 | 11:33,369,553 | A/T | — | uncertain significance |
| rs1853555856 | 11:33,369,741 | A/T | — | uncertain significance |
| rs1590193746 | 11:33,370,084 | A/T | — | uncertain significance |
| rs750454121 | 11:33,370,108 | T/C | — | uncertain significance |
| rs781392443 | 11:33,370,157 | G/A | — | uncertain significance |
| rs781158617 | 11:33,370,183 | T/A | — | uncertain significance |
| rs139168123 | 11:33,370,259 | G/A | — | uncertain significance |
| rs143130710 | 11:33,370,824 | G/T | — | uncertain significance |
| rs142589533 | 11:33,373,216 | C/T | — | uncertain significance |
| rs201982369 | 11:33,373,383 | A/G | — | uncertain significance |
| rs746065570 | 11:33,373,753 | G/T | — | uncertain significance |
| rs2495136587 | 11:33,373,815 | T/G | — | uncertain significance |
| rs572445631 | 11:33,374,726 | G/C | — | uncertain significance |
| rs745497440 | 11:33,374,747 | A/G | — | uncertain significance |
| rs200223965 | 11:33,374,759 | A/G | — | uncertain significance |
| rs149374485 | 11:33,374,777 | C/A | — | uncertain significance |
| rs764431138 | 11:33,374,815 | A/G | — | uncertain significance |
| rs745414263 | 11:33,374,837 | C/T | — | uncertain significance |
| rs2495144549 | 11:33,374,879 | C/T | — | uncertain significance |
| rs768855318 | 11:33,375,071 | T/G | — | uncertain significance |
| rs146182417 | 11:33,375,085 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.