OPRD1
opioid receptor delta 1
Summary
Enables G protein-coupled enkephalin receptor activity. Involved in several processes, including G protein-coupled opioid receptor signaling pathway; cellular response to hypoxia; and positive regulation of peptidyl-serine phosphorylation. Located in plasma membrane. Implicated in alcohol dependence; alcohol use disorder; drug dependence (multiple); opioid abuse; and withdrawal disorder. Biomarker of opioid abuse. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs569356 | 1:29,136,686 | A/G | upstream gene variant | — |
| rs779942585 | 1:29,138,908 | C/T | — | uncertain significance |
| rs777740780 | 1:29,138,936 | C/T | — | uncertain significance |
| rs778538430 | 1:29,138,954 | C/G | — | uncertain significance |
| rs760200668 | 1:29,138,966 | C/T | — | uncertain significance |
| rs1042114 | 1:29,138,975 | G/T | missense variant | — |
| rs1020204624 | 1:29,139,016 | C/T | — | uncertain significance |
| rs750267952 | 1:29,139,088 | C/G | — | uncertain significance |
| rs2236861 | 1:29,139,756 | G/A | regulatory region variant | — |
| rs533123 | 1:29,141,155 | G/A | intron variant | — |
| rs678849 | 1:29,145,188 | C/G | — | — |
| rs6426344 | 1:29,151,444 | C/A | — | — |
| rs590013 | 1:29,155,738 | T/C | intron variant | — |
| rs2236857 | 1:29,161,609 | T/C | intron variant | — |
| rs10799122 | 1:29,168,766 | G/A | — | — |
| rs3766951 | 1:29,169,559 | T/C | intron variant | — |
| rs529520 | 1:29,174,946 | A/G | — | — |
| rs581111 | 1:29,175,373 | A/G | intron variant | — |
| rs12749204 | 1:29,176,213 | A/G | intron variant | — |
| rs937990510 | 1:29,185,545 | C/A | — | uncertain significance |
| rs560311089 | 1:29,185,576 | C/T | — | uncertain significance |
| rs763837018 | 1:29,185,634 | G/C | — | uncertain significance |
| rs530055186 | 1:29,185,716 | C/T | — | uncertain significance |
| rs960113173 | 1:29,189,259 | G/A | — | uncertain significance |
| rs2089135799 | 1:29,189,374 | A/G | — | uncertain significance |
| rs548573683 | 1:29,189,487 | G/T | — | uncertain significance |
| rs2234918 | 1:29,189,597 | C/G | synonymous variant | — |
| rs753737057 | 1:29,189,716 | G/A | — | uncertain significance |
| rs779559537 | 1:29,189,743 | G/A | — | uncertain significance |
| rs751125712 | 1:29,189,758 | C/T | — | uncertain significance |
| rs781771653 | 1:29,189,770 | G/A | — | uncertain significance |
| rs204076 | 1:29,190,390 | T/A | downstream gene variant | — |
| rs204073 | 1:29,192,722 | C/T | regulatory region variant | — |
| rs204070 | 1:29,194,637 | G/T | coding sequence variant | — |
| rs204068 | 1:29,194,913 | A/G | coding sequence variant | — |
| rs204065 | 1:29,195,940 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.