TMEM108
transmembrane protein 108
Summary
Predicted to be involved in several processes, including cellular response to brain-derived neurotrophic factor stimulus; nervous system development; and regulation of signal transduction. Predicted to be located in somatodendritic compartment. Predicted to be active in several cellular components, including endosome; glutamatergic synapse; and postsynaptic density membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9875380 | 3:132,780,356 | C/T | intron variant | — |
| rs9864997 | 3:132,864,471 | T/C | intron variant | — |
| rs192622883 | 3:132,869,407 | A/G | intron variant | — |
| rs575962315 | 3:132,884,214 | C/A | — | — |
| rs183511413 | 3:133,049,262 | A/G | intron variant | — |
| rs1337477635 | 3:133,098,611 | T/C | — | uncertain significance |
| rs2529310617 | 3:133,098,614 | C/A | — | uncertain significance |
| rs367779843 | 3:133,098,622 | G/A | — | uncertain significance |
| rs775227079 | 3:133,098,626 | C/T | — | uncertain significance |
| rs371498992 | 3:133,098,640 | A/G | — | likely benign |
| rs200624038 | 3:133,098,689 | C/T | — | uncertain significance |
| rs779983086 | 3:133,098,742 | G/A | — | uncertain significance |
| rs202042493 | 3:133,098,772 | C/A | — | uncertain significance |
| rs745430893 | 3:133,098,815 | G/A | — | likely benign |
| rs767996292 | 3:133,098,863 | C/T | — | uncertain significance |
| rs143911768 | 3:133,098,871 | G/A | — | likely benign |
| rs981167322 | 3:133,098,911 | C/T | — | uncertain significance |
| rs371885570 | 3:133,098,929 | C/T | — | uncertain significance |
| rs2529313598 | 3:133,098,973 | A/C | — | uncertain significance |
| rs200974256 | 3:133,098,995 | C/T | — | uncertain significance |
| rs35846010 | 3:133,098,996 | G/A | — | benign |
| rs1040483967 | 3:133,099,003 | A/G | — | uncertain significance |
| rs139900505 | 3:133,099,010 | G/A | — | uncertain significance |
| rs376720769 | 3:133,099,025 | C/A | — | uncertain significance |
| rs369853711 | 3:133,099,043 | G/A | — | uncertain significance |
| rs369887303 | 3:133,099,073 | G/A | — | uncertain significance |
| rs947358587 | 3:133,099,118 | G/A | — | uncertain significance |
| rs1262999544 | 3:133,099,172 | C/T | — | uncertain significance |
| rs774872132 | 3:133,099,265 | C/A | — | uncertain significance |
| rs143399570 | 3:133,099,296 | A/G | — | benign |
| rs376604681 | 3:133,099,303 | C/A | — | uncertain significance |
| rs778009590 | 3:133,099,352 | C/T | — | uncertain significance |
| rs2529318907 | 3:133,099,412 | G/A | — | uncertain significance |
| rs535065177 | 3:133,099,583 | G/A | — | likely benign |
| rs145954165 | 3:133,099,631 | C/G | — | uncertain significance |
| rs763308311 | 3:133,099,729 | G/A | — | uncertain significance |
| rs151083377 | 3:133,099,753 | G/A | — | uncertain significance |
| rs149789292 | 3:133,099,793 | G/A | — | uncertain significance |
| rs147035119 | 3:133,099,849 | C/T | — | uncertain significance |
| rs781038773 | 3:133,099,861 | G/A | — | uncertain significance |
| rs375774878 | 3:133,099,864 | G/A | — | uncertain significance |
| rs768000315 | 3:133,099,922 | C/T | — | uncertain significance |
| rs1559942507 | 3:133,099,970 | T/C | — | uncertain significance |
| rs760319960 | 3:133,109,068 | G/A | — | uncertain significance |
| rs1473772712 | 3:133,109,104 | A/G | — | likely benign |
| rs1377011080 | 3:133,114,800 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.