UEVLD
UEV and lactate/malate dehyrogenase domains
Summary
Predicted to enable ubiquitin binding activity. Predicted to be involved in endosome to lysosome transport. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1009171786 | 11:18,553,881 | G/C | — | uncertain significance |
| rs771433671 | 11:18,553,949 | G/A | — | uncertain significance |
| rs1466939018 | 11:18,553,961 | A/G | — | uncertain significance |
| rs765037651 | 11:18,553,994 | G/A | — | uncertain significance |
| rs749678241 | 11:18,555,948 | A/G | — | uncertain significance |
| rs565899539 | 11:18,555,965 | G/A | — | uncertain significance |
| rs775586236 | 11:18,555,975 | C/A | — | uncertain significance |
| rs1281289698 | 11:18,555,982 | T/G | — | uncertain significance |
| rs760469030 | 11:18,558,014 | G/A | — | uncertain significance |
| rs199750985 | 11:18,566,238 | G/A | — | uncertain significance |
| rs150856594 | 11:18,566,292 | C/T | — | uncertain significance |
| rs2495036706 | 11:18,566,329 | A/G | — | uncertain significance |
| rs190084899 | 11:18,566,818 | C/A | intron variant | — |
| rs61752315 | 11:18,568,429 | G/A | — | uncertain significance |
| rs199616488 | 11:18,568,451 | C/T | — | uncertain significance |
| rs1157466636 | 11:18,568,501 | T/C | — | uncertain significance |
| rs1462197897 | 11:18,568,550 | A/C | — | uncertain significance |
| rs2495126782 | 11:18,579,821 | C/T | — | likely benign |
| rs765156441 | 11:18,579,876 | C/T | — | uncertain significance |
| rs367771273 | 11:18,586,461 | C/G | — | uncertain significance |
| rs2495178930 | 11:18,586,494 | G/T | — | uncertain significance |
| rs2495179504 | 11:18,586,547 | A/T | — | uncertain significance |
| rs2495190511 | 11:18,587,935 | C/G | — | uncertain significance |
| rs1852303594 | 11:18,587,950 | G/A | — | uncertain significance |
| rs148829977 | 11:18,587,966 | T/G | — | likely benign |
| rs202218047 | 11:18,588,015 | A/C | — | uncertain significance |
| rs1449721548 | 11:18,591,762 | T/C | — | uncertain significance |
| rs200821433 | 11:18,591,780 | T/C | — | uncertain significance |
| rs532766452 | 11:18,591,783 | G/C | — | uncertain significance |
| rs201825877 | 11:18,591,792 | A/G | — | uncertain significance |
| rs374766407 | 11:18,591,820 | C/T | — | uncertain significance |
| rs536536319 | 11:18,591,844 | T/C | — | uncertain significance |
| rs201991675 | 11:18,591,871 | C/T | — | uncertain significance |
| rs2495219395 | 11:18,591,906 | G/T | — | uncertain significance |
| rs768992780 | 11:18,596,951 | C/T | — | uncertain significance |
| rs1032826278 | 11:18,596,956 | A/G | — | uncertain significance |
| rs777777936 | 11:18,602,436 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.