SSTR5
somatostatin receptor 5
Summary
Somatostatin and its related peptide cortistatin exert multiple biological actions on normal and tumoral tissue targets by interacting with somatostatin receptors (SSTRs). The protein encoded by this gene is one of the SSTRs, which is a multi-pass membrane protein and belongs to the G-protein coupled receptor 1 family. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase, and different regions of this receptor molecule are required for the activation of different signaling pathways. A mutation in this gene results in somatostatin analog resistance. Alternatively spliced transcript variants have been identified in this gene.[provided by RefSeq, Feb 2010]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2548447786 | 16:1,128,893 | A/G | — | uncertain significance |
| rs143790659 | 16:1,128,894 | C/T | — | likely benign |
| rs35128939 | 16:1,128,901 | C/T | — | benign |
| rs146894362 | 16:1,128,908 | G/A | — | likely benign |
| rs760953447 | 16:1,128,918 | C/G | — | uncertain significance |
| rs373197738 | 16:1,128,937 | C/T | — | likely benign |
| rs757810045 | 16:1,128,944 | A/C | — | uncertain significance |
| rs374411583 | 16:1,128,966 | C/T | — | uncertain significance |
| rs202179964 | 16:1,128,972 | C/T | — | uncertain significance |
| rs752514090 | 16:1,128,987 | C/T | — | uncertain significance |
| rs751149190 | 16:1,129,001 | G/A | — | uncertain significance |
| rs4988483 | 16:1,129,010 | C/A | — | benign |
| rs4988485 | 16:1,129,024 | G/A | — | benign |
| rs755773123 | 16:1,129,082 | A/G | — | uncertain significance |
| rs540162038 | 16:1,129,088 | G/A | — | uncertain significance |
| rs761743016 | 16:1,129,161 | C/T | — | uncertain significance |
| rs368008840 | 16:1,129,162 | G/A | — | likely benign |
| rs1201637702 | 16:1,129,176 | C/T | — | uncertain significance |
| rs4988486 | 16:1,129,189 | C/T | — | benign |
| rs910895232 | 16:1,129,205 | C/T | — | uncertain significance |
| rs753466942 | 16:1,129,229 | G/A | — | likely benign |
| rs34654948 | 16:1,129,270 | C/T | — | benign |
| rs373018204 | 16:1,129,278 | G/A | — | uncertain significance |
| rs759226187 | 16:1,129,299 | C/T | — | uncertain significance |
| rs35659646 | 16:1,129,309 | G/A | — | benign |
| rs756590942 | 16:1,129,313 | C/T | — | uncertain significance |
| rs150485280 | 16:1,129,329 | G/A | — | uncertain significance |
| rs35328406 | 16:1,129,351 | C/T | — | benign |
| rs146909462 | 16:1,129,381 | G/A | — | benign |
| rs748931906 | 16:1,129,386 | C/T | — | uncertain significance |
| rs751834151 | 16:1,129,418 | G/A | — | uncertain significance |
| rs565410160 | 16:1,129,430 | G/A | — | uncertain significance |
| rs548054752 | 16:1,129,463 | G/A | — | uncertain significance |
| rs143272280 | 16:1,129,466 | G/A | — | uncertain significance |
| rs2548448433 | 16:1,129,479 | A/C | — | uncertain significance |
| rs371990445 | 16:1,129,502 | G/A | — | uncertain significance |
| rs35798577 | 16:1,129,504 | G/A | — | benign |
| rs4988488 | 16:1,129,525 | G/A | — | benign |
| rs1279658530 | 16:1,129,541 | G/A | — | uncertain significance |
| rs200669734 | 16:1,129,545 | T/C | — | uncertain significance |
| rs35804776 | 16:1,129,561 | G/A | — | likely benign |
| rs149886925 | 16:1,129,569 | G/A | — | uncertain significance |
| rs147160220 | 16:1,129,579 | C/T | — | likely benign |
| rs121917877 | 16:1,129,586 | C/T | missense variant | likely benign |
| rs770790521 | 16:1,129,593 | C/T | — | uncertain significance |
| rs151120448 | 16:1,129,609 | G/A | — | likely benign |
| rs369907643 | 16:1,129,611 | G/A | — | uncertain significance |
| rs775435241 | 16:1,129,676 | G/A | — | uncertain significance |
| rs138864924 | 16:1,129,685 | G/T | — | uncertain significance |
| rs199827607 | 16:1,129,688 | G/A | — | uncertain significance |
| rs942652870 | 16:1,129,718 | G/A | — | uncertain significance |
| rs199907399 | 16:1,129,725 | A/G | — | uncertain significance |
| rs767040883 | 16:1,129,757 | A/G | — | uncertain significance |
| rs764648847 | 16:1,129,772 | G/A | — | uncertain significance |
| rs757340833 | 16:1,129,781 | G/A | — | uncertain significance |
| rs757901409 | 16:1,129,856 | G/A | — | uncertain significance |
| rs12596873 | 16:1,129,866 | C/T | — | benign |
| rs169068 | 16:1,129,872 | C/T | — | benign |
| rs371873453 | 16:1,129,908 | C/G | — | uncertain significance |
| rs762032160 | 16:1,129,925 | G/A | — | uncertain significance |
| rs368135536 | 16:1,129,928 | G/A | — | uncertain significance |
| rs368711005 | 16:1,129,959 | T/C | — | uncertain significance |
| rs197056 | 16:1,131,695 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.