TMC5
transmembrane channel like 5
Summary
Predicted to enable mechanosensitive monoatomic ion channel activity. Predicted to be involved in monoatomic ion transmembrane transport. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201217836 | 16:19,451,544 | C/T | missense variant | — |
| rs750186180 | 16:19,451,783 | C/A | — | likely benign |
| rs772394226 | 16:19,452,028 | C/T | — | uncertain significance |
| rs920660246 | 16:19,471,588 | G/A | — | uncertain significance |
| rs1422996241 | 16:19,471,632 | C/T | — | uncertain significance |
| rs2506524295 | 16:19,471,634 | A/G | — | uncertain significance |
| rs142366138 | 16:19,471,647 | G/A | — | likely benign |
| rs1469889922 | 16:19,475,154 | G/T | — | uncertain significance |
| rs190728673 | 16:19,475,162 | C/T | — | uncertain significance |
| rs377526217 | 16:19,475,174 | T/C | — | uncertain significance |
| rs199934900 | 16:19,475,197 | G/A | — | uncertain significance |
| rs764397430 | 16:19,475,293 | G/A | — | uncertain significance |
| rs373261054 | 16:19,475,304 | G/C | — | uncertain significance |
| rs201340058 | 16:19,477,423 | T/C | — | uncertain significance |
| rs760586337 | 16:19,477,473 | G/A | — | uncertain significance |
| rs142604406 | 16:19,477,477 | C/T | — | uncertain significance |
| rs200661492 | 16:19,477,515 | G/A | — | uncertain significance |
| rs144904444 | 16:19,481,006 | G/A | — | uncertain significance |
| rs371305899 | 16:19,481,052 | G/A | — | likely benign |
| rs1968358825 | 16:19,483,455 | A/G | — | uncertain significance |
| rs142693954 | 16:19,483,470 | C/T | — | uncertain significance |
| rs200596133 | 16:19,483,485 | A/G | — | likely benign |
| rs146026607 | 16:19,483,492 | C/T | — | uncertain significance |
| rs1334495884 | 16:19,483,515 | G/T | — | uncertain significance |
| rs1384049735 | 16:19,485,457 | C/A | — | uncertain significance |
| rs758231421 | 16:19,485,481 | T/C | — | uncertain significance |
| rs767192302 | 16:19,485,561 | G/A | — | uncertain significance |
| rs201085859 | 16:19,485,585 | G/C | — | uncertain significance |
| rs756743579 | 16:19,488,788 | T/C | — | uncertain significance |
| rs769075056 | 16:19,488,820 | G/A | — | uncertain significance |
| rs770960643 | 16:19,490,798 | A/C | — | uncertain significance |
| rs764954347 | 16:19,490,840 | T/C | — | uncertain significance |
| rs776371575 | 16:19,492,715 | C/G | — | uncertain significance |
| rs200637158 | 16:19,492,753 | G/A | — | uncertain significance |
| rs552798789 | 16:19,498,524 | A/G | — | uncertain significance |
| rs970253813 | 16:19,498,540 | C/T | — | uncertain significance |
| rs757969590 | 16:19,498,558 | G/A | — | uncertain significance |
| rs1968768769 | 16:19,498,606 | C/T | — | uncertain significance |
| rs1217266717 | 16:19,498,630 | T/C | — | uncertain significance |
| rs201517116 | 16:19,498,636 | T/C | — | uncertain significance |
| rs138670843 | 16:19,498,639 | C/T | — | uncertain significance |
| rs16972065 | 16:19,499,993 | C/T | regulatory region variant | — |
| rs1968857275 | 16:19,501,752 | G/A | — | uncertain significance |
| rs377463683 | 16:19,501,838 | C/T | — | uncertain significance |
| rs374724962 | 16:19,501,848 | T/C | — | uncertain significance |
| rs765880306 | 16:19,503,488 | T/C | — | uncertain significance |
| rs201955285 | 16:19,505,595 | T/A | — | uncertain significance |
| rs559836452 | 16:19,505,625 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.