SLC7A6
solute carrier family 7 member 6
Summary
Enables L-lysine:L-arginine antiporter activity and arginine binding activity. Involved in L-arginine transmembrane transport; L-leucine transport; and ornithine transport. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs8056893 | 16:68,304,392 | C/A | intron variant | — |
| rs151229239 | 16:68,308,661 | C/T | — | uncertain significance |
| rs553247630 | 16:68,308,674 | T/C | — | likely benign |
| rs62636644 | 16:68,308,707 | A/T | — | benign |
| rs199740573 | 16:68,308,875 | T/G | — | uncertain significance |
| rs140250756 | 16:68,309,058 | C/T | — | likely benign |
| rs1345582896 | 16:68,309,095 | T/C | — | uncertain significance |
| rs143818486 | 16:68,309,129 | G/A | — | uncertain significance |
| rs3785111 | 16:68,309,971 | A/G | — | — |
| rs4783612 | 16:68,312,469 | T/C | — | — |
| rs761175588 | 16:68,321,706 | C/T | — | uncertain significance |
| rs200717924 | 16:68,321,717 | G/A | — | uncertain significance |
| rs199757376 | 16:68,321,736 | T/C | — | uncertain significance |
| rs368252496 | 16:68,324,322 | G/A | — | uncertain significance |
| rs1241334275 | 16:68,324,332 | G/A | — | uncertain significance |
| rs62636648 | 16:68,325,203 | T/A | — | benign |
| rs143127763 | 16:68,325,478 | G/A | — | likely benign |
| rs2543410588 | 16:68,325,501 | T/C | — | uncertain significance |
| rs6499165 | 16:68,326,200 | A/C | intron variant | — |
| rs769826112 | 16:68,328,643 | C/T | — | uncertain significance |
| rs770527629 | 16:68,328,690 | G/C | — | uncertain significance |
| rs79087422 | 16:68,330,397 | A/G | — | likely benign |
| rs140967956 | 16:68,330,402 | C/T | — | uncertain significance |
| rs2543415129 | 16:68,330,562 | A/G | — | uncertain significance |
| rs116107120 | 16:68,330,630 | T/C | — | benign |
| rs923449854 | 16:68,330,683 | C/T | — | uncertain significance |
| rs745413753 | 16:68,330,708 | T/C | — | uncertain significance |
| rs143248146 | 16:68,331,171 | T/C | — | likely benign |
| rs775196374 | 16:68,331,175 | G/A | — | uncertain significance |
| rs201797964 | 16:68,331,179 | T/C | — | uncertain significance |
| rs2863979 | 16:68,331,890 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.