TAAR5
trace amine associated receptor 5
Summary
Enables trimethylamine receptor activity. Involved in adenylate cyclase-activating G protein-coupled receptor signaling pathway. Is active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145127866 | 6:132,909,837 | C/G | — | likely benign |
| rs35839363 | 6:132,909,838 | G/A | — | benign |
| rs201738989 | 6:132,909,865 | T/A | — | uncertain significance |
| rs374357879 | 6:132,909,889 | G/A | — | uncertain significance |
| rs1776852138 | 6:132,909,939 | A/T | — | uncertain significance |
| rs34746740 | 6:132,910,011 | G/A | — | likely benign |
| rs1005810941 | 6:132,910,048 | T/C | — | uncertain significance |
| rs775816647 | 6:132,910,050 | C/A | — | uncertain significance |
| rs2483131406 | 6:132,910,113 | T/C | — | uncertain significance |
| rs2483131422 | 6:132,910,116 | C/A | — | uncertain significance |
| rs745969010 | 6:132,910,137 | G/A | — | uncertain significance |
| rs36116159 | 6:132,910,145 | G/A | — | benign |
| rs751214094 | 6:132,910,209 | G/A | — | uncertain significance |
| rs142528485 | 6:132,910,243 | G/T | — | likely benign |
| rs375488941 | 6:132,910,267 | G/A | — | uncertain significance |
| rs142165413 | 6:132,910,406 | C/G | — | benign |
| rs142040103 | 6:132,910,449 | C/A | — | uncertain significance |
| rs770530202 | 6:132,910,467 | G/A | — | uncertain significance |
| rs150806754 | 6:132,910,469 | G/A | — | likely benign |
| rs1183696401 | 6:132,910,483 | T/C | — | uncertain significance |
| rs372095515 | 6:132,910,503 | C/A | — | uncertain significance |
| rs781004698 | 6:132,910,513 | A/G | — | uncertain significance |
| rs374786875 | 6:132,910,519 | C/T | — | uncertain significance |
| rs917609935 | 6:132,910,531 | A/G | — | uncertain significance |
| rs147867541 | 6:132,910,626 | G/A | — | likely benign |
| rs1461152969 | 6:132,910,669 | C/T | — | uncertain significance |
| rs763077527 | 6:132,910,681 | C/T | — | uncertain significance |
| rs144579755 | 6:132,910,707 | G/T | — | uncertain significance |
| rs111404356 | 6:132,910,710 | A/G | — | uncertain significance |
| rs369553631 | 6:132,910,746 | G/A | — | uncertain significance |
| rs147135761 | 6:132,910,778 | G/A | — | likely benign |
| rs539414366 | 6:132,913,201 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.