TMEM175
transmembrane protein 175
Summary
Enables arachidonate binding activity; potassium ion leak channel activity; and proton channel activity. Involved in lysosomal lumen pH elevation; potassium ion transmembrane transport; and proton transmembrane transport. Located in endosome membrane and lysosome. Is active in lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6599388 | 4:939,087 | C/T | intron variant | — |
| rs6599389 | 4:939,113 | G/A | regulatory region variant | — |
| rs1351585053 | 4:941,532 | C/G | — | uncertain significance |
| rs140775030 | 4:941,541 | G/A | — | likely benign |
| rs1728365808 | 4:941,576 | T/G | — | uncertain significance |
| rs371061303 | 4:941,590 | G/C | — | uncertain significance |
| rs150597099 | 4:941,603 | G/A | — | uncertain significance |
| rs149909734 | 4:941,923 | C/T | — | uncertain significance |
| rs34884217 | 4:944,210 | A/C | — | benign |
| rs151228848 | 4:944,254 | G/A | — | uncertain significance |
| rs754171022 | 4:944,275 | A/C | — | uncertain significance |
| rs1314983139 | 4:944,284 | G/A | — | uncertain significance |
| rs200834686 | 4:945,017 | A/G | — | uncertain significance |
| rs1483599851 | 4:945,023 | G/A | — | uncertain significance |
| rs2533832237 | 4:945,486 | T/A | — | uncertain significance |
| rs766017281 | 4:946,159 | C/T | — | uncertain significance |
| rs11552301 | 4:946,226 | T/C | — | benign |
| rs191845987 | 4:946,228 | G/C | — | uncertain significance |
| rs1188588099 | 4:946,982 | T/C | — | uncertain significance |
| rs201589218 | 4:947,093 | C/T | — | uncertain significance |
| rs142553376 | 4:949,214 | G/A | — | uncertain significance |
| rs555645036 | 4:949,554 | C/T | — | uncertain significance |
| rs147772555 | 4:949,569 | G/C | — | uncertain significance |
| rs561973833 | 4:949,659 | C/T | — | uncertain significance |
| rs368224007 | 4:951,613 | G/A | — | uncertain significance |
| rs139228186 | 4:951,619 | A/G | — | likely benign |
| rs200183497 | 4:951,622 | G/A | — | uncertain significance |
| rs61732682 | 4:951,633 | C/T | — | benign |
| rs200254468 | 4:951,682 | G/A | — | uncertain significance |
| rs199802807 | 4:951,694 | C/T | — | uncertain significance |
| rs762817717 | 4:951,704 | C/A | — | uncertain significance |
| rs573432765 | 4:951,712 | G/A | — | uncertain significance |
| rs143946130 | 4:951,745 | G/A | — | uncertain significance |
| rs149156711 | 4:951,878 | G/A | — | likely benign |
| rs138803304 | 4:951,892 | C/T | — | uncertain significance |
| rs751828848 | 4:951,899 | G/A | — | uncertain significance |
| rs34311866 | 4:951,947 | T/C | missense variant | benign |
| rs202010290 | 4:951,959 | C/T | — | uncertain significance |
| rs1014836665 | 4:951,971 | A/G | — | uncertain significance |
| rs370082052 | 4:951,974 | C/T | — | uncertain significance |
| rs2533891221 | 4:951,989 | C/T | — | uncertain significance |
| rs140597786 | 4:952,009 | C/T | — | likely benign |
| rs1288200328 | 4:952,095 | G/T | — | uncertain significance |
| rs368509864 | 4:952,131 | C/G | — | likely benign |
| rs763288512 | 4:952,141 | G/A | — | uncertain significance |
| rs2533893523 | 4:952,160 | T/C | — | uncertain significance |
| rs747444581 | 4:952,165 | G/A | — | uncertain significance |
| rs144899767 | 4:952,190 | G/A | — | uncertain significance |
| rs368248170 | 4:952,198 | C/T | — | uncertain significance |
| rs1711549874 | 4:952,229 | C/T | — | uncertain significance |
| rs758032940 | 4:952,249 | G/A | — | uncertain significance |
| rs1220872120 | 4:952,268 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.