NTSR1
neurotensin receptor 1
Summary
Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secretion. [provided by RefSeq, Jul 2008]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs763467302 | 20:61,340,584 | G/A | — | uncertain significance |
| rs1470757486 | 20:61,340,591 | C/G | — | uncertain significance |
| rs1170418978 | 20:61,340,624 | C/T | — | uncertain significance |
| rs745837545 | 20:61,340,639 | A/G | — | uncertain significance |
| rs61730136 | 20:61,340,676 | G/A | — | benign |
| rs61742231 | 20:61,340,694 | C/T | — | benign |
| rs543659006 | 20:61,340,720 | T/C | — | uncertain significance |
| rs34257083 | 20:61,340,732 | C/T | — | benign |
| rs11698783 | 20:61,340,774 | C/T | — | benign |
| rs769081526 | 20:61,340,798 | G/A | — | uncertain significance |
| rs375499484 | 20:61,340,854 | A/G | — | uncertain significance |
| rs370549384 | 20:61,340,891 | C/T | — | uncertain significance |
| rs1600715206 | 20:61,340,901 | C/T | — | likely benign |
| rs368494260 | 20:61,341,023 | C/T | — | uncertain significance |
| rs754416393 | 20:61,341,110 | G/T | — | uncertain significance |
| rs868476359 | 20:61,341,203 | A/G | — | uncertain significance |
| rs778351934 | 20:61,341,260 | A/C | — | uncertain significance |
| rs763331199 | 20:61,341,262 | G/A | — | uncertain significance |
| rs4334545 | 20:61,353,177 | C/G | — | — |
| rs6090453 | 20:61,355,362 | C/T | — | — |
| rs6011914 | 20:61,359,351 | C/G | regulatory region variant | — |
| rs2427422 | 20:61,359,973 | G/A | downstream gene variant | — |
| rs3915568 | 20:61,369,472 | T/C | upstream gene variant | — |
| rs556755451 | 20:61,384,965 | G/A | — | — |
| rs201598535 | 20:61,386,100 | G/A | — | uncertain significance |
| rs35373650 | 20:61,386,147 | A/C | — | benign |
| rs546918503 | 20:61,386,166 | G/A | — | uncertain significance |
| rs749500837 | 20:61,386,204 | G/T | — | uncertain significance |
| rs535774214 | 20:61,386,217 | C/T | — | uncertain significance |
| rs34864360 | 20:61,386,225 | C/T | — | benign |
| rs772996912 | 20:61,386,230 | G/A | — | uncertain significance |
| rs59757062 | 20:61,389,612 | C/A | — | benign |
| rs1361136291 | 20:61,389,647 | T/C | — | uncertain significance |
| rs372116403 | 20:61,389,668 | C/T | — | uncertain significance |
| rs113016803 | 20:61,389,691 | G/A | — | likely benign |
| rs139953956 | 20:61,391,378 | A/G | — | benign |
| rs143899545 | 20:61,391,383 | T/C | — | benign |
| rs201959227 | 20:61,391,401 | A/G | — | uncertain significance |
| rs762257928 | 20:61,391,451 | G/A | — | likely benign |
| rs45613333 | 20:61,391,514 | G/A | — | likely benign |
| rs140834874 | 20:61,391,521 | C/T | — | uncertain significance |
| rs73918681 | 20:61,391,524 | C/T | — | benign |
| rs148516370 | 20:61,391,525 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.