SLC22A9
solute carrier family 22 member 9
Summary
Enables short-chain fatty acid transmembrane transporter activity and sodium-independent organic anion transmembrane transporter activity. Involved in hormone transport; short-chain fatty acid transmembrane transport; and sodium-independent organic anion transport. Located in basolateral plasma membrane. Implicated in Lynch syndrome and mismatch repair cancer syndrome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs765887719 | 11:63,137,542 | A/G | — | uncertain significance |
| rs2014323122 | 11:63,137,611 | C/T | — | uncertain significance |
| rs758001813 | 11:63,137,659 | T/C | — | uncertain significance |
| rs746168096 | 11:63,137,713 | A/G | — | uncertain significance |
| rs771616311 | 11:63,137,865 | A/C | — | uncertain significance |
| rs146412511 | 11:63,137,866 | T/C | — | likely benign |
| rs1346341411 | 11:63,137,880 | G/C | — | uncertain significance |
| rs768309551 | 11:63,137,884 | G/T | — | uncertain significance |
| rs1434688636 | 11:63,137,931 | G/A | — | uncertain significance |
| rs148371788 | 11:63,141,207 | T/A | — | uncertain significance |
| rs776740117 | 11:63,141,216 | C/T | — | uncertain significance |
| rs1565181297 | 11:63,141,491 | C/G | — | uncertain significance |
| rs2539381899 | 11:63,143,145 | A/G | — | uncertain significance |
| rs2014449436 | 11:63,143,204 | T/A | — | uncertain significance |
| rs113967277 | 11:63,157,889 | A/G | intron variant | — |
| rs144071365 | 11:63,168,423 | C/A | intron variant | — |
| rs7101446 | 11:63,173,684 | T/A | — | — |
| rs2539417495 | 11:63,174,069 | C/G | — | uncertain significance |
| rs760458545 | 11:63,174,115 | G/T | — | uncertain significance |
| rs765961866 | 11:63,174,118 | C/G | — | uncertain significance |
| rs532350906 | 11:63,174,127 | T/C | — | uncertain significance |
| rs1471304807 | 11:63,174,129 | C/T | — | uncertain significance |
| rs761599956 | 11:63,175,628 | G/A | — | uncertain significance |
| rs755395828 | 11:63,175,647 | C/A | — | uncertain significance |
| rs146027075 | 11:63,176,187 | A/G | missense variant | — |
| rs11231455 | 11:63,176,494 | G/C | intron variant | — |
| rs773707960 | 11:63,177,281 | G/A | — | uncertain significance |
| rs2539423113 | 11:63,177,330 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.