SLC16A11
solute carrier family 16 member 11
Summary
Enables pyruvate transmembrane transporter activity. Involved in lipid metabolic process. Located in endoplasmic reticulum membrane and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1016367289 | 17:6,945,060 | C/T | — | uncertain significance |
| rs75493593 | 17:6,945,087 | G/C | missense variant | — |
| rs368479181 | 17:6,945,114 | C/G | — | likely benign |
| rs776500476 | 17:6,945,117 | A/T | — | uncertain significance |
| rs138521125 | 17:6,945,159 | C/G | — | uncertain significance |
| rs372509336 | 17:6,945,191 | G/A | — | uncertain significance |
| rs377215105 | 17:6,945,341 | C/T | — | uncertain significance |
| rs761962811 | 17:6,945,363 | C/G | — | uncertain significance |
| rs778536344 | 17:6,945,405 | C/G | — | uncertain significance |
| rs763205831 | 17:6,945,464 | G/A | — | uncertain significance |
| rs75418188 | 17:6,945,483 | C/A | missense variant | — |
| rs547077705 | 17:6,945,525 | C/T | — | uncertain significance |
| rs1442055165 | 17:6,945,668 | C/T | — | uncertain significance |
| rs200478682 | 17:6,945,669 | C/T | — | uncertain significance |
| rs1484890245 | 17:6,945,677 | C/G | — | uncertain significance |
| rs1400235240 | 17:6,945,713 | A/G | — | uncertain significance |
| rs1193232489 | 17:6,945,720 | G/A | — | uncertain significance |
| rs865782605 | 17:6,945,732 | C/T | — | uncertain significance |
| rs2507868385 | 17:6,945,746 | G/C | — | uncertain significance |
| rs751237232 | 17:6,945,749 | G/C | — | uncertain significance |
| rs372321938 | 17:6,945,788 | A/G | — | uncertain significance |
| rs376947673 | 17:6,945,819 | G/A | — | uncertain significance |
| rs759252457 | 17:6,945,843 | G/T | — | uncertain significance |
| rs377196600 | 17:6,945,900 | C/A | — | uncertain significance |
| rs768736062 | 17:6,945,914 | G/T | — | uncertain significance |
| rs2507869072 | 17:6,945,932 | G/A | — | uncertain significance |
| rs1346651796 | 17:6,945,935 | T/A | — | uncertain significance |
| rs199684329 | 17:6,945,936 | C/G | — | uncertain significance |
| rs13342232 | 17:6,945,940 | A/G | synonymous variant | — |
| rs753353144 | 17:6,945,971 | G/A | — | uncertain significance |
| rs755152407 | 17:6,946,044 | T/C | — | uncertain significance |
| rs761467841 | 17:6,946,266 | C/A | — | uncertain significance |
| rs769188847 | 17:6,946,278 | T/C | — | uncertain significance |
| rs13342692 | 17:6,946,287 | T/C | missense variant | benign |
| rs557902498 | 17:6,946,288 | C/A | — | uncertain significance |
| rs752869402 | 17:6,946,314 | C/T | — | uncertain significance |
| rs117767867 | 17:6,946,330 | C/T | missense variant | — |
| rs373049645 | 17:6,946,348 | C/A | — | uncertain significance |
| rs753934775 | 17:6,946,386 | A/G | — | uncertain significance |
| rs371508899 | 17:6,946,390 | G/A | — | uncertain significance |
| rs759591467 | 17:6,946,641 | C/A | — | uncertain significance |
| rs772525806 | 17:6,946,684 | G/A | — | uncertain significance |
| rs1597348024 | 17:6,946,703 | C/T | — | uncertain significance |
| rs757941446 | 17:6,946,754 | G/C | — | uncertain significance |
| rs574004862 | 17:6,946,828 | G/A | — | uncertain significance |
| rs2292351 | 17:6,946,921 | C/G | regulatory region variant | — |
| rs74577409 | 17:6,947,453 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.