CCKAR
cholecystokinin A receptor
Summary
This gene encodes a G-protein coupled receptor that binds non-sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776397508 | 4:26,483,285 | A/T | — | uncertain significance |
| rs2475450432 | 4:26,483,345 | C/T | — | uncertain significance |
| rs754280360 | 4:26,483,448 | G/T | — | uncertain significance |
| rs52795588 | 4:26,483,454 | C/T | missense variant | benign |
| rs200830872 | 4:26,483,462 | G/T | — | uncertain significance |
| rs114925681 | 4:26,483,513 | C/T | — | uncertain significance |
| rs115488558 | 4:26,483,526 | C/T | — | uncertain significance |
| rs199510290 | 4:26,483,548 | G/T | — | uncertain significance |
| rs778956662 | 4:26,483,553 | C/T | — | uncertain significance |
| rs2475450925 | 4:26,483,568 | T/C | — | uncertain significance |
| rs202061123 | 4:26,483,654 | C/A | — | uncertain significance |
| rs140102483 | 4:26,483,748 | C/T | — | uncertain significance |
| rs143678945 | 4:26,483,751 | T/C | — | uncertain significance |
| rs200826139 | 4:26,484,838 | T/C | — | uncertain significance |
| rs773043148 | 4:26,484,881 | G/A | — | likely benign |
| rs370015751 | 4:26,484,900 | G/C | — | uncertain significance |
| rs191275118 | 4:26,486,282 | A/G | intron variant | — |
| rs776531003 | 4:26,487,310 | G/A | — | uncertain significance |
| rs1418064018 | 4:26,487,315 | G/T | — | uncertain significance |
| rs115021107 | 4:26,487,361 | G/A | — | uncertain significance |
| rs202000988 | 4:26,487,436 | C/G | — | uncertain significance |
| rs74671182 | 4:26,487,460 | G/A | — | uncertain significance |
| rs1192489202 | 4:26,487,506 | C/T | — | uncertain significance |
| rs202206580 | 4:26,490,866 | G/A | — | uncertain significance |
| rs943601131 | 4:26,490,935 | A/G | — | uncertain significance |
| rs146802844 | 4:26,491,056 | T/C | — | uncertain significance |
| rs1800857 | 4:26,491,111 | A/T | — | — |
| rs1800855 | 4:26,491,117 | A/T | intron variant | — |
| rs200494718 | 4:26,491,781 | T/C | — | uncertain significance |
| rs770111352 | 4:26,491,822 | T/C | — | uncertain significance |
| rs104893833 | 4:26,491,829 | C/G | missense variant | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.