IPO4
importin 4
Summary
Enables nuclear import signal receptor activity and nuclear localization sequence binding activity. Involved in protein import into nucleus. Located in chromatin. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370925111 | 14:24,649,665 | C/T | — | uncertain significance |
| rs2039114140 | 14:24,649,686 | T/C | — | uncertain significance |
| rs1438987136 | 14:24,649,745 | A/G | — | uncertain significance |
| rs756375329 | 14:24,650,762 | A/G | — | uncertain significance |
| rs565997832 | 14:24,650,999 | C/T | — | uncertain significance |
| rs760631161 | 14:24,651,186 | C/T | — | uncertain significance |
| rs2039146411 | 14:24,651,232 | G/C | — | uncertain significance |
| rs758144689 | 14:24,651,327 | T/C | — | uncertain significance |
| rs778273518 | 14:24,651,491 | C/G | — | uncertain significance |
| rs201215254 | 14:24,651,492 | A/G | — | uncertain significance |
| rs202112878 | 14:24,651,513 | C/T | — | uncertain significance |
| rs2039153516 | 14:24,651,535 | G/C | — | uncertain significance |
| rs2502145003 | 14:24,652,190 | G/C | — | uncertain significance |
| rs1398067357 | 14:24,652,192 | A/G | — | uncertain significance |
| rs747787561 | 14:24,652,208 | C/T | — | likely benign |
| rs200223765 | 14:24,652,310 | G/A | — | uncertain significance |
| rs367855911 | 14:24,652,315 | C/T | — | uncertain significance |
| rs372694223 | 14:24,652,349 | C/T | — | uncertain significance |
| rs201084822 | 14:24,652,354 | C/T | — | uncertain significance |
| rs1266294667 | 14:24,652,492 | C/T | — | uncertain significance |
| rs775364818 | 14:24,652,531 | G/A | — | uncertain significance |
| rs921633468 | 14:24,652,552 | G/C | — | uncertain significance |
| rs560973696 | 14:24,652,700 | T/C | — | uncertain significance |
| rs1340673712 | 14:24,652,711 | A/C | — | uncertain significance |
| rs202114287 | 14:24,652,813 | C/T | — | likely benign |
| rs749026018 | 14:24,652,818 | C/G | — | uncertain significance |
| rs369678433 | 14:24,652,821 | C/T | — | uncertain significance |
| rs774810094 | 14:24,652,852 | G/C | — | uncertain significance |
| rs761179222 | 14:24,652,863 | C/G | — | uncertain significance |
| rs2502147571 | 14:24,653,008 | C/T | — | uncertain significance |
| rs184433827 | 14:24,653,066 | G/A | — | benign |
| rs1245876167 | 14:24,653,092 | C/T | — | uncertain significance |
| rs540493054 | 14:24,653,215 | C/T | — | uncertain significance |
| rs753184356 | 14:24,653,244 | G/A | — | uncertain significance |
| rs559669192 | 14:24,653,268 | G/A | — | uncertain significance |
| rs780298284 | 14:24,653,538 | C/T | — | likely benign |
| rs769903817 | 14:24,653,579 | G/A | — | uncertain significance |
| rs546882621 | 14:24,653,657 | G/A | — | — |
| rs368932351 | 14:24,653,943 | G/A | — | uncertain significance |
| rs199521914 | 14:24,653,947 | C/T | — | likely benign |
| rs375884071 | 14:24,653,951 | G/A | — | uncertain significance |
| rs566741453 | 14:24,654,088 | C/T | — | uncertain significance |
| rs1387143297 | 14:24,654,106 | T/C | — | uncertain significance |
| rs145779241 | 14:24,654,115 | G/T | — | benign |
| rs2502153697 | 14:24,654,688 | C/T | — | uncertain significance |
| rs768754715 | 14:24,654,693 | G/A | — | uncertain significance |
| rs374190960 | 14:24,654,712 | G/A | — | uncertain significance |
| rs533823461 | 14:24,654,723 | G/A | — | uncertain significance |
| rs1264709377 | 14:24,654,738 | C/A | — | uncertain significance |
| rs367677423 | 14:24,654,752 | C/A | — | uncertain significance |
| rs745749457 | 14:24,654,760 | G/T | — | uncertain significance |
| rs375733777 | 14:24,655,148 | C/T | — | uncertain significance |
| rs1360539172 | 14:24,655,154 | A/G | — | uncertain significance |
| rs776015389 | 14:24,655,355 | C/G | — | uncertain significance |
| rs1276427428 | 14:24,655,361 | G/A | — | uncertain significance |
| rs367756147 | 14:24,655,515 | G/A | — | uncertain significance |
| rs768094321 | 14:24,656,118 | G/C | — | uncertain significance |
| rs763348892 | 14:24,656,125 | T/G | — | uncertain significance |
| rs370544113 | 14:24,656,185 | C/T | — | uncertain significance |
| rs2502162657 | 14:24,656,628 | G/A | — | uncertain significance |
| rs202050737 | 14:24,656,649 | C/T | — | uncertain significance |
| rs201377584 | 14:24,656,684 | C/G | — | uncertain significance |
| rs2502163384 | 14:24,656,727 | T/C | — | uncertain significance |
| rs541325634 | 14:24,656,893 | G/A | — | uncertain significance |
| rs772824423 | 14:24,656,939 | C/A | — | uncertain significance |
| rs767082261 | 14:24,656,955 | C/T | — | uncertain significance |
| rs369071941 | 14:24,657,456 | A/T | — | uncertain significance |
| rs745699521 | 14:24,657,559 | T/G | — | uncertain significance |
| rs369567721 | 14:24,657,565 | G/A | — | uncertain significance |
| rs747596805 | 14:24,657,577 | C/T | — | uncertain significance |
| rs751437225 | 14:24,657,774 | G/A | — | uncertain significance |
| rs780946673 | 14:24,657,781 | G/T | — | uncertain significance |
| rs1189426749 | 14:24,657,832 | G/A | — | uncertain significance |
| rs114902352 | 14:24,657,936 | G/A | — | benign |
| rs542303871 | 14:24,657,963 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.