GPR155
G protein-coupled receptor 155
Summary
Enables cholesterol binding activity. Involved in several processes, including cellular response to amino acid starvation; cellular response to cholesterol; and positive regulation of TORC1 signaling. Located in extracellular exosome. Is active in lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1396514235 | 2:175,300,858 | A/T | — | uncertain significance |
| rs780838905 | 2:175,300,918 | C/T | — | uncertain significance |
| rs528682867 | 2:175,300,984 | G/A | — | uncertain significance |
| rs138579883 | 2:175,300,992 | T/C | — | uncertain significance |
| rs966660402 | 2:175,301,059 | C/T | — | uncertain significance |
| rs200743346 | 2:175,301,062 | G/A | — | uncertain significance |
| rs201833095 | 2:175,301,078 | G/A | — | likely benign |
| rs376052691 | 2:175,301,090 | C/A | — | uncertain significance |
| rs775917213 | 2:175,301,139 | C/T | — | uncertain significance |
| rs12995528 | 2:175,303,245 | G/C | intron variant | — |
| rs558267349 | 2:175,304,647 | C/T | — | likely benign |
| rs745614550 | 2:175,304,662 | C/T | — | uncertain significance |
| rs2468242561 | 2:175,304,737 | T/G | — | uncertain significance |
| rs78653158 | 2:175,304,760 | A/G | — | benign |
| rs76781804 | 2:175,306,885 | T/C | — | benign |
| rs759641655 | 2:175,311,356 | T/C | — | uncertain significance |
| rs1481802501 | 2:175,311,472 | T/C | — | uncertain significance |
| rs370036675 | 2:175,324,620 | G/C | — | uncertain significance |
| rs745662483 | 2:175,324,656 | G/A | — | uncertain significance |
| rs762888833 | 2:175,324,714 | C/T | — | uncertain significance |
| rs1170192326 | 2:175,324,759 | T/C | — | uncertain significance |
| rs78053572 | 2:175,324,781 | G/A | — | benign |
| rs1327140322 | 2:175,324,785 | C/T | — | uncertain significance |
| rs142543316 | 2:175,324,786 | T/C | — | uncertain significance |
| rs779866292 | 2:175,324,813 | T/C | — | uncertain significance |
| rs751398281 | 2:175,326,135 | C/T | — | uncertain significance |
| rs1687692034 | 2:175,326,189 | T/G | — | uncertain significance |
| rs199785525 | 2:175,326,338 | T/C | — | uncertain significance |
| rs1687699552 | 2:175,326,349 | A/C | — | uncertain significance |
| rs1687823165 | 2:175,330,539 | G/A | — | uncertain significance |
| rs2468301808 | 2:175,330,582 | T/A | — | uncertain significance |
| rs756589877 | 2:175,330,594 | C/A | — | uncertain significance |
| rs759745513 | 2:175,331,298 | G/A | — | uncertain significance |
| rs1687915275 | 2:175,333,683 | T/G | — | uncertain significance |
| rs75119523 | 2:175,333,732 | A/G | — | benign |
| rs371272111 | 2:175,333,744 | C/T | — | uncertain significance |
| rs374491850 | 2:175,335,226 | A/C | — | uncertain significance |
| rs2468312491 | 2:175,335,257 | T/G | — | uncertain significance |
| rs369296052 | 2:175,337,779 | A/C | — | uncertain significance |
| rs369595816 | 2:175,337,856 | G/C | — | uncertain significance |
| rs199560893 | 2:175,337,898 | T/C | — | uncertain significance |
| rs2468318769 | 2:175,337,908 | T/A | — | uncertain significance |
| rs541458587 | 2:175,337,922 | G/T | — | uncertain significance |
| rs1688048485 | 2:175,337,934 | C/A | — | uncertain significance |
| rs138596030 | 2:175,338,074 | G/A | — | likely benign |
| rs1248350432 | 2:175,346,257 | T/A | — | uncertain significance |
| rs761267379 | 2:175,346,488 | G/A | — | uncertain significance |
| rs373785524 | 2:175,346,576 | T/C | — | uncertain significance |
| rs747987926 | 2:175,346,602 | A/C | — | uncertain significance |
| rs139805062 | 2:175,346,630 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.