PKN2
protein kinase N2
Summary
Enables RNA polymerase binding activity; histone deacetylase binding activity; and protein serine/threonine kinase activity. Involved in several processes, including apical junction assembly; positive regulation of cell cycle; and positive regulation of viral genome replication. Located in several cellular components, including cleavage furrow; cytoskeleton; and midbody. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35492837 | 1:89,153,855 | A/C | — | — |
| rs167365 | 1:89,180,845 | C/G | intron variant | — |
| rs305226 | 1:89,186,565 | A/T | — | — |
| rs565452751 | 1:89,188,820 | A/G | — | — |
| rs369171613 | 1:89,206,681 | G/A | — | uncertain significance |
| rs375306359 | 1:89,206,690 | C/T | — | uncertain significance |
| rs199689449 | 1:89,206,740 | A/G | — | likely benign |
| rs305219 | 1:89,210,859 | C/T | intron variant | — |
| rs305217 | 1:89,220,472 | G/A | intron variant | — |
| rs749956821 | 1:89,225,944 | G/T | — | uncertain significance |
| rs1421789734 | 1:89,225,979 | C/A | — | uncertain significance |
| rs12021820 | 1:89,231,763 | T/A | intron variant | — |
| rs634683 | 1:89,232,337 | G/T | intron variant | — |
| rs1669892191 | 1:89,237,149 | G/A | — | uncertain significance |
| rs373232178 | 1:89,237,506 | G/C | — | uncertain significance |
| rs780702051 | 1:89,237,512 | T/C | — | uncertain significance |
| rs759522341 | 1:89,237,530 | A/G | — | uncertain significance |
| rs150661383 | 1:89,238,781 | A/G | intron variant | — |
| rs805047 | 1:89,242,372 | A/C | — | — |
| rs786923 | 1:89,242,954 | C/T | intron variant | — |
| rs201111346 | 1:89,250,359 | C/G | — | uncertain significance |
| rs1670502762 | 1:89,250,443 | G/A | — | uncertain significance |
| rs758934826 | 1:89,250,468 | G/A | — | uncertain significance |
| rs371274223 | 1:89,250,478 | G/A | — | uncertain significance |
| rs377562198 | 1:89,251,862 | C/T | — | uncertain significance |
| rs786908 | 1:89,253,357 | A/G | intron variant | — |
| rs201149414 | 1:89,271,299 | C/T | — | uncertain significance |
| rs369266668 | 1:89,271,308 | G/A | — | uncertain significance |
| rs761591652 | 1:89,271,327 | G/A | — | uncertain significance |
| rs954278016 | 1:89,271,620 | C/A | — | uncertain significance |
| rs377246617 | 1:89,271,636 | G/A | — | uncertain significance |
| rs761087281 | 1:89,271,641 | T/G | — | uncertain significance |
| rs769594034 | 1:89,273,012 | T/C | — | uncertain significance |
| rs376189560 | 1:89,273,247 | T/G | — | uncertain significance |
| rs1265040340 | 1:89,273,257 | T/G | — | uncertain significance |
| rs2524094787 | 1:89,273,389 | A/G | — | uncertain significance |
| rs1253381552 | 1:89,273,401 | T/C | — | uncertain significance |
| rs786919 | 1:89,281,529 | A/G | upstream gene variant | — |
| rs1085563 | 1:89,284,108 | G/A | — | — |
| rs2524175040 | 1:89,290,040 | A/C | — | uncertain significance |
| rs754548194 | 1:89,294,173 | A/G | — | uncertain significance |
| rs786913 | 1:89,295,330 | A/C | — | — |
| rs786914 | 1:89,295,765 | C/A | downstream gene variant | — |
| rs370637742 | 1:89,298,523 | A/G | — | uncertain significance |
| rs1672796203 | 1:89,298,773 | A/G | — | uncertain significance |
| rs1672797194 | 1:89,298,787 | C/G | — | uncertain significance |
| rs765126182 | 1:89,298,943 | G/A | — | uncertain significance |
| rs2524215047 | 1:89,299,068 | G/C | — | uncertain significance |
| rs200905692 | 1:89,299,076 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.