TMEM145
transmembrane protein 145
Summary
Predicted to be involved in G protein-coupled receptor signaling pathway and response to pheromone. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs111871714 | 19:42,817,176 | G/C | regulatory region variant | — |
| rs1238722347 | 19:42,817,532 | G/A | — | uncertain significance |
| rs1414161978 | 19:42,817,544 | G/T | — | uncertain significance |
| rs1288620763 | 19:42,817,569 | C/T | — | uncertain significance |
| rs982969477 | 19:42,817,602 | C/G | — | uncertain significance |
| rs2514203336 | 19:42,817,628 | G/A | — | uncertain significance |
| rs2514203433 | 19:42,817,644 | A/T | — | uncertain significance |
| rs751810337 | 19:42,818,431 | T/A | — | uncertain significance |
| rs768887283 | 19:42,818,480 | C/G | — | uncertain significance |
| rs1262708043 | 19:42,818,619 | A/G | — | uncertain significance |
| rs769767615 | 19:42,819,206 | G/A | — | uncertain significance |
| rs200045960 | 19:42,819,217 | G/A | — | uncertain significance |
| rs1243143077 | 19:42,819,345 | C/G | — | uncertain significance |
| rs202212359 | 19:42,819,369 | C/T | — | uncertain significance |
| rs774005845 | 19:42,819,389 | C/G | — | uncertain significance |
| rs527465607 | 19:42,819,539 | G/A | — | uncertain significance |
| rs765422940 | 19:42,821,047 | G/A | — | uncertain significance |
| rs2514212485 | 19:42,821,080 | C/T | — | uncertain significance |
| rs762133267 | 19:42,821,111 | C/T | — | uncertain significance |
| rs2514214508 | 19:42,821,931 | T/A | — | uncertain significance |
| rs376219157 | 19:42,822,024 | A/G | — | uncertain significance |
| rs142071177 | 19:42,823,128 | C/T | intron variant | — |
| rs370100137 | 19:42,824,509 | G/C | — | uncertain significance |
| rs753778493 | 19:42,824,510 | G/A | — | uncertain significance |
| rs1186436135 | 19:42,824,534 | A/C | — | uncertain significance |
| rs773733094 | 19:42,824,572 | G/A | — | uncertain significance |
| rs746197610 | 19:42,827,798 | G/A | — | uncertain significance |
| rs767211706 | 19:42,827,861 | G/A | — | uncertain significance |
| rs760922463 | 19:42,827,865 | A/G | — | uncertain significance |
| rs768867486 | 19:42,827,919 | C/T | — | uncertain significance |
| rs143263887 | 19:42,827,927 | C/G | — | uncertain significance |
| rs2514225421 | 19:42,827,936 | A/T | — | likely benign |
| rs540616003 | 19:42,828,943 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.