SLC46A2
solute carrier family 46 member 2
Summary
Enables cyclic-GMP-AMP transmembrane transporter activity. Involved in cyclic-GMP-AMP transmembrane import across plasma membrane and positive regulation of nucleotide-binding activity oligomerization domain containing 1 signaling pathway. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs56024259 | 9:115,640,979 | G/A | downstream gene variant | — |
| rs778157773 | 9:115,642,055 | A/G | — | uncertain significance |
| rs2490881866 | 9:115,648,753 | T/C | — | uncertain significance |
| rs761459250 | 9:115,648,779 | A/G | — | uncertain significance |
| rs1320103301 | 9:115,648,800 | A/G | — | uncertain significance |
| rs148125885 | 9:115,648,885 | C/T | — | uncertain significance |
| rs749047937 | 9:115,649,618 | G/C | — | uncertain significance |
| rs145175372 | 9:115,651,183 | T/G | downstream gene variant | — |
| rs16917454 | 9:115,651,865 | G/A | — | benign |
| rs188435024 | 9:115,651,886 | C/T | — | uncertain significance |
| rs761965885 | 9:115,651,925 | C/T | — | likely benign |
| rs766244345 | 9:115,651,946 | A/G | — | uncertain significance |
| rs376496916 | 9:115,651,950 | C/T | — | uncertain significance |
| rs558581867 | 9:115,652,055 | C/A | — | uncertain significance |
| rs777976291 | 9:115,652,058 | C/T | — | uncertain significance |
| rs1423434735 | 9:115,652,091 | T/C | — | uncertain significance |
| rs1228510323 | 9:115,652,120 | G/A | — | uncertain significance |
| rs377646939 | 9:115,652,168 | T/C | — | likely benign |
| rs7021942 | 9:115,652,185 | A/G | — | benign |
| rs764973566 | 9:115,652,201 | C/T | — | uncertain significance |
| rs7022287 | 9:115,652,203 | G/A | — | benign |
| rs114822090 | 9:115,652,236 | G/A | — | benign |
| rs199687345 | 9:115,652,274 | G/A | — | uncertain significance |
| rs368719760 | 9:115,652,319 | A/T | — | uncertain significance |
| rs2490889491 | 9:115,652,327 | C/G | — | uncertain significance |
| rs1336190496 | 9:115,652,447 | C/T | — | uncertain significance |
| rs1180535599 | 9:115,652,474 | C/G | — | uncertain significance |
| rs148598559 | 9:115,652,573 | T/C | — | uncertain significance |
| rs1209388899 | 9:115,652,624 | A/G | — | uncertain significance |
| rs1299140630 | 9:115,652,648 | C/G | — | uncertain significance |
| rs1227334948 | 9:115,652,651 | T/G | — | uncertain significance |
| rs111494276 | 9:115,652,678 | C/T | — | uncertain significance |
| rs761575386 | 9:115,652,699 | G/A | — | uncertain significance |
| rs1282006067 | 9:115,652,712 | C/T | — | uncertain significance |
| rs371414131 | 9:115,652,744 | G/A | — | uncertain significance |
| rs1434980421 | 9:115,652,847 | C/T | — | uncertain significance |
| rs946884406 | 9:115,652,850 | C/T | — | uncertain significance |
| rs200301213 | 9:115,652,865 | C/T | — | uncertain significance |
| rs770678832 | 9:115,652,889 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.