SLC36A3
solute carrier family 36 member 3
Summary
Predicted to enable amino acid transmembrane transporter activity. Predicted to be involved in carboxylic acid transport and proton transmembrane transport. Predicted to be located in membrane. Predicted to be active in vacuolar membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs532280240 | 5:150,656,989 | G/A | — | uncertain significance |
| rs2531778117 | 5:150,657,066 | A/G | — | uncertain significance |
| rs776172852 | 5:150,657,088 | C/T | — | uncertain significance |
| rs1018843282 | 5:150,657,141 | A/T | — | uncertain significance |
| rs375681986 | 5:150,657,166 | C/T | — | uncertain significance |
| rs147738288 | 5:150,657,199 | G/A | — | uncertain significance |
| rs137940541 | 5:150,658,762 | G/T | intron variant | — |
| rs10061997 | 5:150,658,987 | T/C | intron variant | — |
| rs201585244 | 5:150,660,598 | C/T | — | uncertain significance |
| rs142309332 | 5:150,660,599 | G/A | — | uncertain significance |
| rs370559654 | 5:150,660,655 | G/A | — | uncertain significance |
| rs151230457 | 5:150,660,710 | C/T | — | uncertain significance |
| rs535145820 | 5:150,660,735 | C/G | — | uncertain significance |
| rs768483360 | 5:150,663,609 | A/G | — | uncertain significance |
| rs375214964 | 5:150,664,206 | T/C | — | uncertain significance |
| rs748087930 | 5:150,664,239 | C/T | — | uncertain significance |
| rs779708024 | 5:150,666,835 | A/G | — | uncertain significance |
| rs763420005 | 5:150,666,851 | T/C | — | uncertain significance |
| rs111989476 | 5:150,666,868 | G/A | — | uncertain significance |
| rs778720370 | 5:150,666,884 | C/G | — | uncertain significance |
| rs754478122 | 5:150,666,906 | C/A | — | uncertain significance |
| rs1421393735 | 5:150,666,951 | G/T | — | uncertain significance |
| rs137910049 | 5:150,666,974 | G/T | — | uncertain significance |
| rs142449284 | 5:150,667,007 | C/T | — | uncertain significance |
| rs2531837717 | 5:150,672,952 | C/A | — | uncertain significance |
| rs369042266 | 5:150,672,962 | G/A | — | uncertain significance |
| rs199990744 | 5:150,672,967 | G/A | — | uncertain significance |
| rs144585535 | 5:150,672,982 | A/G | — | uncertain significance |
| rs150561602 | 5:150,672,988 | G/T | — | uncertain significance |
| rs2531838281 | 5:150,673,010 | T/G | — | uncertain significance |
| rs190240877 | 5:150,673,405 | C/T | regulatory region variant | — |
| rs750544349 | 5:150,675,790 | C/T | — | uncertain significance |
| rs150945002 | 5:150,678,162 | C/T | — | uncertain significance |
| rs757040190 | 5:150,678,230 | A/G | — | uncertain significance |
| rs375819646 | 5:150,682,797 | G/C | — | uncertain significance |
| rs145383818 | 5:150,682,801 | C/T | — | uncertain significance |
| rs184972022 | 5:150,682,836 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.