UBXN6
UBX domain protein 6
Summary
Enables ATPase binding activity. Involved in ERAD pathway; endosome to lysosome transport via multivesicular body sorting pathway; and macroautophagy. Located in bounding membrane of organelle and cytosol. Part of endosome and protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138129036 | 19:4,445,527 | C/T | — | uncertain significance |
| rs1345649979 | 19:4,445,549 | C/G | — | uncertain significance |
| rs749462877 | 19:4,445,551 | C/T | — | uncertain significance |
| rs77077573 | 19:4,445,559 | G/A | — | uncertain significance |
| rs200555890 | 19:4,445,581 | C/T | — | uncertain significance |
| rs538086106 | 19:4,445,584 | C/T | — | uncertain significance |
| rs775713602 | 19:4,446,156 | C/A | — | uncertain significance |
| rs201322182 | 19:4,446,358 | T/C | — | uncertain significance |
| rs781219649 | 19:4,446,378 | C/T | — | uncertain significance |
| rs756313078 | 19:4,446,381 | A/G | — | uncertain significance |
| rs375533590 | 19:4,446,385 | C/G | — | uncertain significance |
| rs201517666 | 19:4,446,393 | C/A | — | uncertain significance |
| rs776268944 | 19:4,446,394 | G/A | — | uncertain significance |
| rs532929768 | 19:4,446,536 | T/C | — | uncertain significance |
| rs765248393 | 19:4,446,538 | G/T | — | uncertain significance |
| rs147606668 | 19:4,446,564 | G/T | — | uncertain significance |
| rs151060057 | 19:4,446,615 | C/T | — | uncertain significance |
| rs201394926 | 19:4,446,618 | G/A | — | uncertain significance |
| rs8101961 | 19:4,446,629 | G/A | — | uncertain significance |
| rs1199999286 | 19:4,446,648 | T/C | — | uncertain significance |
| rs200898701 | 19:4,446,680 | G/C | — | uncertain significance |
| rs200629893 | 19:4,446,683 | G/C | — | uncertain significance |
| rs138342613 | 19:4,446,871 | A/G | — | uncertain significance |
| rs149610347 | 19:4,446,888 | G/A | — | likely benign |
| rs758984301 | 19:4,446,914 | G/A | — | uncertain significance |
| rs2512337707 | 19:4,446,916 | T/C | — | uncertain significance |
| rs367786829 | 19:4,447,588 | C/T | — | uncertain significance |
| rs141391502 | 19:4,447,594 | C/T | — | uncertain significance |
| rs376182636 | 19:4,447,598 | G/T | — | uncertain significance |
| rs2145173399 | 19:4,447,603 | G/C | — | uncertain significance |
| rs756042421 | 19:4,448,366 | G/A | — | uncertain significance |
| rs200775962 | 19:4,452,441 | C/T | — | uncertain significance |
| rs765934867 | 19:4,452,482 | T/C | — | uncertain significance |
| rs411833 | 19:4,453,325 | G/C | downstream gene variant | — |
| rs1158225949 | 19:4,453,462 | G/C | — | uncertain significance |
| rs764525926 | 19:4,453,484 | C/T | — | uncertain significance |
| rs1164747388 | 19:4,453,508 | G/A | — | uncertain significance |
| rs533927912 | 19:4,453,950 | G/A | — | uncertain significance |
| rs200291730 | 19:4,453,969 | G/A | — | uncertain significance |
| rs1974700595 | 19:4,454,002 | C/T | — | uncertain significance |
| rs576544561 | 19:4,454,040 | C/T | — | uncertain significance |
| rs780595977 | 19:4,454,055 | G/A | — | uncertain significance |
| rs1127888 | 19:4,454,083 | C/T | missense variant | — |
| rs747449598 | 19:4,457,637 | C/T | — | uncertain significance |
| rs183356732 | 19:4,458,656 | G/A | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.