UBE2Q2
ubiquitin conjugating enzyme E2 Q2
Summary
Enables ubiquitin-protein transferase activity. Involved in protein K48-linked ubiquitination. Predicted to be located in cytosol. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2505241730 | 15:76,136,083 | A/G | — | uncertain significance |
| rs751906868 | 15:76,136,104 | G/C | — | uncertain significance |
| rs778344721 | 15:76,136,118 | G/C | — | uncertain significance |
| rs202209762 | 15:76,136,155 | C/T | — | uncertain significance |
| rs374352758 | 15:76,136,159 | C/G | — | uncertain significance |
| rs532168863 | 15:76,136,674 | G/A | regulatory region variant | — |
| rs60846313 | 15:76,144,194 | A/G | intron variant | — |
| rs750889339 | 15:76,146,727 | G/A | — | uncertain significance |
| rs1205704852 | 15:76,146,764 | A/G | — | uncertain significance |
| rs148604284 | 15:76,146,799 | C/T | — | uncertain significance |
| rs76030018 | 15:76,146,800 | G/A | — | uncertain significance |
| rs748376950 | 15:76,146,815 | A/G | — | uncertain significance |
| rs376429875 | 15:76,152,246 | T/C | — | uncertain significance |
| rs1897123411 | 15:76,152,249 | G/A | — | uncertain significance |
| rs1304836436 | 15:76,152,263 | A/T | — | uncertain significance |
| rs755614652 | 15:76,152,306 | C/T | — | uncertain significance |
| rs370564605 | 15:76,152,313 | C/A | — | uncertain significance |
| rs1462695035 | 15:76,152,321 | C/G | — | uncertain significance |
| rs1394125 | 15:76,158,983 | G/T | — | — |
| rs1976748 | 15:76,160,951 | A/G | intron variant | — |
| rs1365911036 | 15:76,161,343 | A/G | — | uncertain significance |
| rs189395301 | 15:76,164,062 | G/T | regulatory region variant | — |
| rs371805905 | 15:76,165,812 | C/G | — | uncertain significance |
| rs768516583 | 15:76,165,841 | G/A | — | uncertain significance |
| rs764421447 | 15:76,168,579 | A/G | — | uncertain significance |
| rs541229832 | 15:76,170,319 | C/G | — | uncertain significance |
| rs1029742438 | 15:76,170,335 | T/C | — | uncertain significance |
| rs750193694 | 15:76,171,447 | C/T | — | uncertain significance |
| rs144579048 | 15:76,171,466 | T/A | — | uncertain significance |
| rs371786099 | 15:76,175,708 | A/G | — | uncertain significance |
| rs2505454298 | 15:76,178,058 | G/A | — | uncertain significance |
| rs148920865 | 15:76,182,801 | T/G | — | uncertain significance |
| rs1029220038 | 15:76,183,281 | A/G | — | uncertain significance |
| rs72734546 | 15:76,188,703 | G/T | downstream gene variant | — |
| rs766738526 | 15:76,189,337 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.