SLC16A9
solute carrier family 16 member 9
Summary
Enables carnitine transmembrane transporter activity and creatine transmembrane transporter activity. Involved in carnitine transmembrane transport; creatine transmembrane transport; and urate metabolic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1465936047 | 10:61,412,535 | C/T | — | uncertain significance |
| rs138607526 | 10:61,412,559 | C/A | — | benign |
| rs2492137682 | 10:61,412,585 | T/G | — | uncertain significance |
| rs1359306953 | 10:61,412,610 | G/T | — | uncertain significance |
| rs1332229564 | 10:61,412,618 | G/A | — | uncertain significance |
| rs371841243 | 10:61,412,679 | C/A | — | uncertain significance |
| rs12356193 | 10:61,413,353 | A/G | intron variant | — |
| rs77799409 | 10:61,413,497 | G/C | — | benign |
| rs770089674 | 10:61,413,519 | G/A | — | uncertain significance |
| rs754998000 | 10:61,413,549 | C/A | — | uncertain significance |
| rs750417619 | 10:61,413,588 | G/C | — | uncertain significance |
| rs2492150369 | 10:61,413,636 | C/T | — | uncertain significance |
| rs2492152436 | 10:61,413,804 | A/G | — | uncertain significance |
| rs761027162 | 10:61,413,829 | C/T | — | uncertain significance |
| rs199889507 | 10:61,413,832 | T/C | — | uncertain significance |
| rs2242206 | 10:61,414,011 | G/T | missense variant | — |
| rs759040496 | 10:61,414,038 | T/C | — | uncertain significance |
| rs999940296 | 10:61,414,072 | A/G | — | uncertain significance |
| rs1006940777 | 10:61,414,102 | G/T | — | uncertain significance |
| rs2492157619 | 10:61,414,200 | T/C | — | uncertain significance |
| rs2492157952 | 10:61,414,233 | C/T | — | uncertain significance |
| rs368640774 | 10:61,414,340 | G/T | — | uncertain significance |
| rs777494122 | 10:61,424,063 | A/C | — | uncertain significance |
| rs11006681 | 10:61,429,527 | G/A | intron variant | — |
| rs754510245 | 10:61,432,549 | A/G | — | uncertain significance |
| rs1439287796 | 10:61,432,562 | G/C | — | uncertain significance |
| rs778609342 | 10:61,432,586 | C/T | — | uncertain significance |
| rs201592301 | 10:61,432,660 | T/C | — | uncertain significance |
| rs753658419 | 10:61,432,671 | C/T | — | uncertain significance |
| rs2492346517 | 10:61,443,930 | C/A | — | uncertain significance |
| rs747303668 | 10:61,444,033 | G/A | — | uncertain significance |
| rs7094971 | 10:61,449,564 | A/G | intron variant | — |
| rs35209863 | 10:61,450,121 | T/C | intron variant | — |
| rs1171650 | 10:61,450,153 | C/A | — | — |
| rs10993963 | 10:61,453,455 | G/C | intron variant | — |
| rs1171620 | 10:61,464,507 | C/T | — | — |
| rs1171617 | 10:61,467,182 | G/T | intron variant | — |
| rs1171615 | 10:61,469,090 | C/G | — | — |
| rs1171614 | 10:61,469,538 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.