DPY19L3
dpy-19 like C-mannosyltransferase 3
Summary
Enables mannosyltransferase activity. Predicted to be involved in protein glycosylation. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10405382 | 19:32,896,716 | C/G | regulatory region variant | — |
| rs10409264 | 19:32,896,846 | G/C | — | — |
| rs375042614 | 19:32,899,169 | A/C | — | uncertain significance |
| rs2513269735 | 19:32,899,238 | A/G | — | uncertain significance |
| rs150957517 | 19:32,902,201 | G/T | — | uncertain significance |
| rs17832737 | 19:32,912,622 | A/G | regulatory region variant | — |
| rs2111504 | 19:32,917,455 | T/A | intron variant | — |
| rs199864417 | 19:32,923,706 | G/A | — | likely benign |
| rs2513338844 | 19:32,928,167 | C/G | — | uncertain significance |
| rs1411457041 | 19:32,930,074 | C/G | — | uncertain significance |
| rs756980403 | 19:32,930,116 | G/C | — | uncertain significance |
| rs746399509 | 19:32,930,799 | A/G | — | uncertain significance |
| rs68013007 | 19:32,938,681 | A/G | — | — |
| rs143976902 | 19:32,940,476 | T/C | intron variant | — |
| rs923298047 | 19:32,944,099 | A/G | — | uncertain significance |
| rs766792616 | 19:32,944,144 | A/G | — | uncertain significance |
| rs1488886020 | 19:32,945,864 | G/A | — | likely benign |
| rs1969821067 | 19:32,945,873 | A/G | — | uncertain significance |
| rs1969821832 | 19:32,945,906 | T/C | — | uncertain significance |
| rs1345965975 | 19:32,945,926 | T/C | — | uncertain significance |
| rs745702094 | 19:32,945,938 | A/G | — | uncertain significance |
| rs144319074 | 19:32,949,022 | A/G | — | uncertain significance |
| rs148643513 | 19:32,949,258 | G/A | — | uncertain significance |
| rs1305199355 | 19:32,949,391 | T/G | — | uncertain significance |
| rs151165240 | 19:32,949,411 | C/T | — | uncertain significance |
| rs4805761 | 19:32,951,800 | A/G | intron variant | — |
| rs12985929 | 19:32,951,841 | G/T | — | — |
| rs10403559 | 19:32,953,101 | T/A | intron variant | — |
| rs748599340 | 19:32,954,291 | T/C | — | uncertain significance |
| rs2513417238 | 19:32,954,339 | G/A | — | uncertain significance |
| rs1256963812 | 19:32,954,353 | A/G | — | uncertain significance |
| rs759015016 | 19:32,955,685 | T/C | — | uncertain significance |
| rs200027601 | 19:32,955,688 | A/G | — | uncertain significance |
| rs2513432703 | 19:32,959,644 | C/T | — | uncertain significance |
| rs749175795 | 19:32,968,450 | G/A | — | uncertain significance |
| rs374961658 | 19:32,968,454 | T/C | — | uncertain significance |
| rs35258637 | 19:32,968,760 | C/T | intron variant | — |
| rs750678080 | 19:32,971,316 | A/G | — | uncertain significance |
| rs1970638195 | 19:32,971,353 | C/G | — | uncertain significance |
| rs34621086 | 19:32,971,377 | G/A | — | uncertain significance |
| rs375213407 | 19:32,971,420 | G/A | — | uncertain significance |
| rs2513455741 | 19:32,971,459 | G/A | — | uncertain significance |
| rs34610265 | 19:32,972,777 | G/A | intron variant | — |
| rs1970691828 | 19:32,973,040 | G/A | — | uncertain significance |
| rs150686956 | 19:32,973,070 | C/T | — | uncertain significance |
| rs746916888 | 19:32,973,078 | G/A | — | likely benign |
| rs766771488 | 19:32,973,140 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.