ADCY9
adenylate cyclase 9
Summary
Adenylate cyclase is a membrane bound enzyme that catalyses the formation of cyclic AMP from ATP. It is regulated by a family of G protein-coupled receptors, protein kinases, and calcium. The type 9 adenylyl cyclase is a widely distributed adenylyl cyclase, and it is stimulated by beta-adrenergic receptor activation but is insensitive to forskolin, calcium, and somatostatin. [provided by RefSeq, Jul 2008]
Known Variants104 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs78843654 | 16:4,004,181 | T/C | — | — |
| rs2531995 | 16:4,013,467 | C/T | 3 prime UTR variant | — |
| rs2238435 | 16:4,014,282 | C/T | — | — |
| rs1045475 | 16:4,015,316 | A/T | — | — |
| rs759474569 | 16:4,015,876 | C/T | — | uncertain significance |
| rs2505573359 | 16:4,015,902 | C/A | — | uncertain significance |
| rs1299789359 | 16:4,015,909 | C/A | — | uncertain significance |
| rs375515956 | 16:4,015,994 | C/T | — | uncertain significance |
| rs768729134 | 16:4,016,038 | T/C | — | uncertain significance |
| rs773282474 | 16:4,016,050 | C/T | — | uncertain significance |
| rs773264079 | 16:4,016,129 | T/C | — | uncertain significance |
| rs778892072 | 16:4,016,234 | C/T | — | uncertain significance |
| rs200368797 | 16:4,016,316 | G/A | — | likely benign |
| rs144864117 | 16:4,016,345 | C/T | — | likely benign |
| rs74003478 | 16:4,016,355 | G/A | — | benign |
| rs781677508 | 16:4,016,401 | A/G | — | uncertain significance |
| rs776481614 | 16:4,016,443 | T/C | — | uncertain significance |
| rs1278100124 | 16:4,016,456 | C/T | — | uncertain significance |
| rs114568080 | 16:4,016,508 | G/A | — | benign |
| rs146978463 | 16:4,016,556 | C/G | — | uncertain significance |
| rs964742894 | 16:4,016,675 | C/A | — | uncertain significance |
| rs2056001007 | 16:4,016,740 | C/G | — | uncertain significance |
| rs143722912 | 16:4,016,844 | G/A | — | likely benign |
| rs757255747 | 16:4,016,874 | G/T | — | likely benign |
| rs545959256 | 16:4,016,933 | G/A | — | uncertain significance |
| rs769823999 | 16:4,016,940 | C/G | — | likely benign |
| rs2230741 | 16:4,016,943 | A/G | synonymous variant | — |
| rs2505577425 | 16:4,016,954 | G/T | — | uncertain significance |
| rs950171987 | 16:4,024,683 | C/G | — | uncertain significance |
| rs1044390225 | 16:4,024,695 | G/C | — | uncertain significance |
| rs2072346 | 16:4,027,423 | C/T | intron variant | — |
| rs149752018 | 16:4,027,479 | G/C | — | likely benign |
| rs1176556124 | 16:4,027,490 | G/C | — | uncertain significance |
| rs768273214 | 16:4,027,495 | A/G | — | uncertain significance |
| rs74003485 | 16:4,027,536 | G/A | — | benign |
| rs2505599815 | 16:4,027,570 | T/G | — | uncertain significance |
| rs150826321 | 16:4,027,595 | C/T | — | uncertain significance |
| rs57040218 | 16:4,027,596 | G/A | — | benign |
| rs912752455 | 16:4,027,606 | G/A | — | likely benign |
| rs749507415 | 16:4,027,611 | C/T | — | likely benign |
| rs371510808 | 16:4,028,562 | A/C | — | — |
| rs372821407 | 16:4,029,125 | T/C | — | uncertain significance |
| rs116402482 | 16:4,029,164 | G/A | — | benign |
| rs144986362 | 16:4,029,167 | C/T | — | uncertain significance |
| rs747260152 | 16:4,029,185 | T/G | — | uncertain significance |
| rs748430579 | 16:4,029,281 | G/A | — | likely benign |
| rs376170586 | 16:4,033,223 | C/T | — | likely benign |
| rs1459120707 | 16:4,033,249 | G/A | — | uncertain significance |
| rs777113575 | 16:4,033,315 | T/C | — | likely benign |
| rs2230739 | 16:4,033,436 | T/A | synonymous variant | — |
| rs2444217 | 16:4,038,387 | G/A | regulatory region variant | — |
| rs756874601 | 16:4,039,017 | T/C | — | uncertain significance |
| rs746910984 | 16:4,039,063 | T/C | — | uncertain significance |
| rs201116391 | 16:4,042,211 | G/C | — | uncertain significance |
| rs759286668 | 16:4,042,295 | T/G | — | uncertain significance |
| rs763995166 | 16:4,042,331 | C/T | — | uncertain significance |
| rs113187435 | 16:4,043,415 | T/C | — | benign |
| rs370853116 | 16:4,043,466 | C/T | — | uncertain significance |
| rs780834261 | 16:4,043,496 | C/T | — | uncertain significance |
| rs2505658165 | 16:4,057,401 | C/T | — | uncertain significance |
| rs1382301876 | 16:4,057,466 | C/T | — | uncertain significance |
| rs1597160753 | 16:4,057,490 | A/G | — | uncertain significance |
| rs144065949 | 16:4,057,515 | G/A | — | likely benign |
| rs778307855 | 16:4,057,517 | G/A | — | uncertain significance |
| rs1967309 | 16:4,065,583 | A/T | — | — |
| rs8052751 | 16:4,081,138 | T/C | upstream gene variant | — |
| rs2601828 | 16:4,103,871 | T/C | regulatory region variant | — |
| rs11076805 | 16:4,106,788 | C/T | — | — |
| rs12598529 | 16:4,120,076 | G/T | — | — |
| rs2601812 | 16:4,124,108 | G/T | intron variant | — |
| rs11647570 | 16:4,137,262 | A/G | intron variant | — |
| rs2247580 | 16:4,137,771 | G/A | regulatory region variant | — |
| rs2601823 | 16:4,141,233 | C/T | intron variant | — |
| rs2601825 | 16:4,141,728 | T/C | intron variant | — |
| rs52791170 | 16:4,163,754 | T/G | — | likely benign |
| rs149348178 | 16:4,163,779 | G/T | — | benign |
| rs2057129152 | 16:4,163,820 | G/A | — | uncertain significance |
| rs765960096 | 16:4,163,831 | T/C | — | uncertain significance |
| rs565530412 | 16:4,163,835 | T/C | — | uncertain significance |
| rs374682488 | 16:4,163,866 | G/A | — | likely benign |
| rs762008865 | 16:4,164,022 | C/A | — | uncertain significance |
| rs1422823034 | 16:4,164,027 | T/C | — | uncertain significance |
| rs2057132526 | 16:4,164,230 | T/C | — | uncertain significance |
| rs1159195754 | 16:4,164,347 | G/C | — | uncertain significance |
| rs780726526 | 16:4,164,425 | C/A | — | uncertain significance |
| rs2057134265 | 16:4,164,448 | C/A | — | uncertain significance |
| rs1439974261 | 16:4,164,509 | T/C | — | uncertain significance |
| rs1426708299 | 16:4,164,584 | A/G | — | uncertain significance |
| rs148841917 | 16:4,164,631 | C/T | — | benign |
| rs2505591306 | 16:4,164,728 | T/G | — | uncertain significance |
| rs752324868 | 16:4,164,736 | G/A | — | likely benign |
| rs1400222331 | 16:4,164,744 | G/A | — | uncertain significance |
| rs201211738 | 16:4,164,756 | C/T | — | uncertain significance |
| rs1309416274 | 16:4,164,788 | G/A | — | uncertain significance |
| rs372461075 | 16:4,164,801 | C/A | — | uncertain significance |
| rs2057138279 | 16:4,164,866 | T/C | — | uncertain significance |
| rs142649683 | 16:4,164,920 | G/A | — | uncertain significance |
| rs3730099 | 16:4,164,955 | G/A | — | benign |
| rs760401817 | 16:4,165,013 | A/C | — | uncertain significance |
| rs200248947 | 16:4,165,032 | T/G | — | uncertain significance |
Showing 100 of 104 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.