ADORA2B
adenosine A2b receptor
Summary
This gene encodes an adenosine receptor that is a member of the G protein-coupled receptor superfamily. This integral membrane protein stimulates adenylate cyclase activity in the presence of adenosine. This protein also interacts with netrin-1, which is involved in axon elongation. The gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs859267 | 17:15,826,021 | A/G | — | — |
| rs2535599 | 17:15,828,161 | G/T | — | — |
| rs759669984 | 17:15,848,585 | C/A | — | uncertain significance |
| rs753144286 | 17:15,848,588 | T/C | — | uncertain significance |
| rs953320326 | 17:15,848,633 | G/A | — | uncertain significance |
| rs61755963 | 17:15,848,666 | C/T | — | benign |
| rs148714288 | 17:15,848,673 | T/C | — | benign |
| rs1257695844 | 17:15,848,687 | C/T | — | uncertain significance |
| rs142739933 | 17:15,848,690 | A/C | — | uncertain significance |
| rs781359164 | 17:15,848,815 | G/T | — | uncertain significance |
| rs1192235636 | 17:15,848,885 | G/A | — | uncertain significance |
| rs1970226843 | 17:15,877,997 | A/C | — | uncertain significance |
| rs79073029 | 17:15,878,011 | G/A | — | benign |
| rs765095998 | 17:15,878,066 | G/A | — | uncertain significance |
| rs2549895279 | 17:15,878,092 | C/G | — | uncertain significance |
| rs775766252 | 17:15,878,234 | C/T | — | uncertain significance |
| rs1203760263 | 17:15,878,262 | A/T | — | uncertain significance |
| rs770185409 | 17:15,878,266 | T/G | — | uncertain significance |
| rs753335309 | 17:15,878,423 | G/A | — | uncertain significance |
| rs2549896133 | 17:15,878,436 | A/G | — | uncertain significance |
| rs73978574 | 17:15,878,443 | T/C | — | benign |
| rs746063928 | 17:15,878,487 | T/G | — | uncertain significance |
| rs544202480 | 17:15,878,541 | G/A | — | uncertain significance |
| rs762496834 | 17:15,878,585 | C/T | — | uncertain significance |
| rs1276230728 | 17:15,878,625 | G/A | — | uncertain significance |
| rs1860645 | 17:15,879,344 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.