ADCY8
adenylate cyclase 8
Summary
Adenylate cyclase is a membrane bound enzyme that catalyses the formation of cyclic AMP from ATP. The enzymatic activity is under the control of several hormones, and different polypeptides participate in the transduction of the signal from the receptor to the catalytic moiety. Stimulatory or inhibitory receptors (Rs and Ri) interact with G proteins (Gs and Gi) that exhibit GTPase activity and they modulate the activity of the catalytic subunit of the adenylyl cyclase [provided by RefSeq, Jul 2008]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs981604557 | 8:131,792,710 | G/A | — | uncertain significance |
| rs201701737 | 8:131,792,712 | C/T | — | uncertain significance |
| rs147371587 | 8:131,792,780 | A/G | — | benign |
| rs139593989 | 8:131,792,810 | C/T | — | benign |
| rs773491638 | 8:131,792,811 | G/A | — | uncertain significance |
| rs573772081 | 8:131,792,812 | C/T | — | uncertain significance |
| rs750136473 | 8:131,792,859 | G/T | — | uncertain significance |
| rs78439900 | 8:131,792,860 | G/C | — | uncertain significance |
| rs1021550886 | 8:131,792,920 | T/A | — | uncertain significance |
| rs771008212 | 8:131,792,936 | C/G | — | uncertain significance |
| rs199631888 | 8:131,792,943 | C/T | — | uncertain significance |
| rs1563660678 | 8:131,793,010 | C/T | — | uncertain significance |
| rs2488473554 | 8:131,793,016 | C/A | — | uncertain significance |
| rs1259673084 | 8:131,796,000 | C/T | — | uncertain significance |
| rs767432306 | 8:131,796,024 | A/G | — | uncertain significance |
| rs2488477763 | 8:131,796,045 | C/T | — | uncertain significance |
| rs1196041156 | 8:131,796,047 | C/T | — | uncertain significance |
| rs263232 | 8:131,808,169 | C/A | intron variant | — |
| rs263238 | 8:131,812,033 | G/T | — | — |
| rs62640023 | 8:131,812,756 | C/T | — | benign |
| rs1586425865 | 8:131,812,783 | C/T | — | likely benign |
| rs765672223 | 8:131,826,347 | G/A | — | uncertain significance |
| rs79196788 | 8:131,859,737 | G/A | — | uncertain significance |
| rs140797450 | 8:131,880,138 | C/T | — | uncertain significance |
| rs770084286 | 8:131,896,837 | C/T | — | uncertain significance |
| rs2488670445 | 8:131,896,841 | A/G | — | uncertain significance |
| rs1438445728 | 8:131,916,247 | C/T | — | uncertain significance |
| rs545028650 | 8:131,916,248 | C/T | — | uncertain significance |
| rs370063278 | 8:131,916,265 | G/A | — | uncertain significance |
| rs12547243 | 8:131,921,956 | A/G | splice region variant | — |
| rs1023960046 | 8:131,921,958 | G/A | — | uncertain significance |
| rs369373540 | 8:131,922,043 | G/A | — | likely benign |
| rs780241069 | 8:131,955,607 | C/T | — | uncertain significance |
| rs769416849 | 8:131,964,178 | C/T | — | uncertain significance |
| rs373225005 | 8:131,964,216 | C/T | — | uncertain significance |
| rs750072698 | 8:131,964,223 | G/A | — | uncertain significance |
| rs138524416 | 8:131,964,240 | C/T | — | uncertain significance |
| rs2536710794 | 8:132,002,725 | A/G | — | uncertain significance |
| rs7824021 | 8:132,005,870 | G/T | intron variant | — |
| rs12678691 | 8:132,010,340 | A/G | intron variant | — |
| rs75269509 | 8:132,051,635 | G/A | — | benign |
| rs199902296 | 8:132,051,701 | G/C | — | uncertain significance |
| rs965094308 | 8:132,051,703 | T/A | — | uncertain significance |
| rs1370708931 | 8:132,051,711 | G/A | — | uncertain significance |
| rs367613298 | 8:132,051,799 | C/T | — | uncertain significance |
| rs1363304398 | 8:132,051,889 | C/G | — | uncertain significance |
| rs554994778 | 8:132,052,021 | C/A | — | uncertain significance |
| rs766740204 | 8:132,052,065 | C/A | — | uncertain significance |
| rs772046627 | 8:132,052,144 | C/A | — | uncertain significance |
| rs754763494 | 8:132,052,234 | C/A | — | uncertain significance |
| rs761355331 | 8:132,052,236 | C/T | — | uncertain significance |
| rs375176511 | 8:132,052,251 | G/T | — | uncertain significance |
| rs372280558 | 8:132,052,284 | C/T | — | uncertain significance |
| rs999968249 | 8:132,052,305 | T/A | — | uncertain significance |
| rs1245348649 | 8:132,052,320 | G/A | — | uncertain significance |
| rs778700013 | 8:132,052,324 | C/A | — | uncertain significance |
| rs1040715439 | 8:132,052,365 | G/T | — | uncertain significance |
| rs571946527 | 8:132,052,369 | G/C | — | uncertain significance |
| rs773033725 | 8:132,052,386 | G/C | — | uncertain significance |
| rs1009420520 | 8:132,052,417 | G/A | — | uncertain significance |
| rs763836127 | 8:132,052,450 | G/T | — | uncertain significance |
| rs531517274 | 8:132,052,492 | C/A | — | uncertain significance |
| rs770681340 | 8:132,052,501 | C/G | — | uncertain significance |
| rs764602731 | 8:132,052,507 | C/T | — | uncertain significance |
| rs2536815798 | 8:132,052,573 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.