IPO9
importin 9
Summary
Enables histone binding activity; histone chaperone activity; and nuclear import signal receptor activity. Involved in proteasome localization and protein import into nucleus. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2644109 | 1:201,797,535 | C/T | downstream gene variant | — |
| rs1189581863 | 1:201,798,371 | G/A | — | uncertain significance |
| rs752546546 | 1:201,798,374 | C/A | — | uncertain significance |
| rs2494114 | 1:201,801,011 | C/G | downstream gene variant | — |
| rs77635059 | 1:201,808,507 | G/A | regulatory region variant | — |
| rs2526712930 | 1:201,817,600 | C/T | — | uncertain significance |
| rs372891944 | 1:201,821,241 | G/T | — | uncertain significance |
| rs375791538 | 1:201,821,254 | C/G | — | uncertain significance |
| rs375241905 | 1:201,823,750 | G/A | — | uncertain significance |
| rs1192309255 | 1:201,823,834 | G/A | — | uncertain significance |
| rs1490520412 | 1:201,824,284 | A/T | — | uncertain significance |
| rs2526728554 | 1:201,824,287 | T/A | — | uncertain significance |
| rs761742745 | 1:201,824,962 | A/G | — | uncertain significance |
| rs772836297 | 1:201,824,967 | C/A | — | uncertain significance |
| rs765881694 | 1:201,824,983 | A/T | — | uncertain significance |
| rs2678207 | 1:201,825,277 | C/T | intron variant | — |
| rs146088439 | 1:201,825,822 | G/A | intron variant | — |
| rs777425167 | 1:201,828,116 | C/T | — | uncertain significance |
| rs200231992 | 1:201,832,599 | G/T | — | uncertain significance |
| rs549731118 | 1:201,832,685 | C/G | — | uncertain significance |
| rs61743350 | 1:201,835,906 | G/A | — | benign |
| rs781370407 | 1:201,835,919 | A/G | — | uncertain significance |
| rs370638350 | 1:201,835,959 | G/C | — | uncertain significance |
| rs2526755737 | 1:201,835,977 | T/G | — | uncertain significance |
| rs757494161 | 1:201,836,018 | G/A | — | uncertain significance |
| rs757623300 | 1:201,837,781 | G/A | — | uncertain significance |
| rs1355907948 | 1:201,837,833 | C/G | — | uncertain significance |
| rs1391897187 | 1:201,837,923 | C/T | — | uncertain significance |
| rs747564859 | 1:201,839,838 | G/T | — | uncertain significance |
| rs775661561 | 1:201,839,871 | G/A | — | uncertain significance |
| rs749013226 | 1:201,840,431 | A/G | — | uncertain significance |
| rs369658460 | 1:201,842,023 | C/T | — | uncertain significance |
| rs2526769364 | 1:201,842,036 | A/T | — | uncertain significance |
| rs778640930 | 1:201,842,072 | G/A | — | uncertain significance |
| rs148953528 | 1:201,843,378 | A/G | — | uncertain significance |
| rs370826445 | 1:201,843,447 | A/G | — | uncertain significance |
| rs757744754 | 1:201,843,457 | G/T | — | uncertain significance |
| rs766333425 | 1:201,843,467 | G/A | — | uncertain significance |
| rs2526775039 | 1:201,843,998 | G/A | — | uncertain significance |
| rs8024 | 1:201,845,575 | C/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.