DPY19L1
dpy-19 like C-mannosyltransferase 1
Summary
Predicted to enable mannosyltransferase activity. Predicted to be involved in protein glycosylation. Located in membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2546869211 | 7:34,971,217 | C/T | — | uncertain significance |
| rs763651855 | 7:34,971,294 | T/C | — | uncertain significance |
| rs917031 | 7:34,972,940 | A/C | intron variant | — |
| rs200311128 | 7:34,977,612 | C/A | — | uncertain significance |
| rs1208881844 | 7:34,977,667 | G/C | — | uncertain significance |
| rs767108874 | 7:34,977,672 | C/T | — | likely benign |
| rs764567538 | 7:34,977,696 | C/T | — | uncertain significance |
| rs1177737159 | 7:34,977,718 | T/C | — | uncertain significance |
| rs1042610257 | 7:34,978,894 | C/G | — | uncertain significance |
| rs1459750571 | 7:34,979,811 | C/A | — | uncertain significance |
| rs904370015 | 7:34,979,831 | C/T | — | uncertain significance |
| rs2546874461 | 7:34,979,836 | T/C | — | uncertain significance |
| rs771903272 | 7:34,979,896 | A/G | — | uncertain significance |
| rs763091779 | 7:34,987,274 | C/T | — | uncertain significance |
| rs1784355006 | 7:34,994,922 | A/G | — | uncertain significance |
| rs755438512 | 7:34,994,951 | A/G | — | uncertain significance |
| rs374462284 | 7:34,997,616 | A/C | — | uncertain significance |
| rs2546885049 | 7:34,997,618 | G/A | — | uncertain significance |
| rs370260184 | 7:34,997,640 | T/C | — | uncertain significance |
| rs756416097 | 7:35,006,508 | T/C | — | uncertain significance |
| rs565383734 | 7:35,009,137 | T/G | — | uncertain significance |
| rs775841504 | 7:35,029,531 | C/G | — | uncertain significance |
| rs1420593740 | 7:35,050,161 | G/A | — | uncertain significance |
| rs372533265 | 7:35,051,008 | T/C | — | uncertain significance |
| rs1396002193 | 7:35,053,198 | T/A | — | uncertain significance |
| rs2546909394 | 7:35,053,289 | A/G | — | uncertain significance |
| rs329238 | 7:35,057,190 | A/G | intron variant | — |
| rs770626492 | 7:35,057,510 | G/A | — | uncertain significance |
| rs762478422 | 7:35,057,549 | C/T | — | uncertain significance |
| rs2546912104 | 7:35,058,193 | A/G | — | uncertain significance |
| rs329269 | 7:35,074,130 | G/C | intron variant | — |
| rs1283607802 | 7:35,077,432 | C/T | — | uncertain significance |
| rs1786486308 | 7:35,077,469 | G/A | — | uncertain significance |
| rs1311576401 | 7:35,077,475 | G/A | — | uncertain significance |
| rs1786487587 | 7:35,077,485 | T/G | — | uncertain significance |
| rs329274 | 7:35,078,743 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.