SLC7A8
solute carrier family 7 member 8
Summary
Enables several functions, including neutral L-amino acid transmembrane transporter activity; protein heterodimerization activity; and secondary active transmembrane transporter activity. Involved in L-alanine import across plasma membrane; L-leucine import across plasma membrane; and thyroid hormone transport. Located in basolateral plasma membrane and microvillus membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1347544956 | 14:23,596,432 | G/C | — | uncertain significance |
| rs771270900 | 14:23,596,442 | T/C | — | uncertain significance |
| rs530953668 | 14:23,596,495 | C/T | — | likely benign |
| rs140596505 | 14:23,596,522 | C/A | — | uncertain significance |
| rs2501840635 | 14:23,597,234 | A/T | — | uncertain significance |
| rs2048595204 | 14:23,597,256 | G/C | — | uncertain significance |
| rs773856869 | 14:23,597,272 | C/A | — | uncertain significance |
| rs2048614085 | 14:23,598,915 | C/G | — | uncertain significance |
| rs749809601 | 14:23,598,963 | G/T | — | uncertain significance |
| rs752410256 | 14:23,599,008 | A/C | — | uncertain significance |
| rs760437691 | 14:23,600,708 | C/T | — | uncertain significance |
| rs768054260 | 14:23,607,178 | G/A | — | uncertain significance |
| rs201546442 | 14:23,608,645 | G/A | — | likely benign |
| rs374741332 | 14:23,608,689 | C/T | — | uncertain significance |
| rs759951698 | 14:23,608,694 | T/C | — | likely pathogenic |
| rs2501877111 | 14:23,609,713 | T/C | — | uncertain significance |
| rs2501877173 | 14:23,609,729 | C/T | — | uncertain significance |
| rs752482499 | 14:23,609,738 | C/T | — | likely pathogenic |
| rs1470081163 | 14:23,609,765 | C/G | — | uncertain significance |
| rs145886415 | 14:23,609,774 | C/T | — | uncertain significance |
| rs540015976 | 14:23,612,381 | G/A | — | uncertain significance |
| rs2501884160 | 14:23,612,399 | C/T | — | uncertain significance |
| rs144511756 | 14:23,614,659 | C/A | intron variant | — |
| rs748339188 | 14:23,634,556 | G/A | — | uncertain significance |
| rs374870578 | 14:23,634,566 | C/T | — | uncertain significance |
| rs745847298 | 14:23,634,583 | A/G | — | uncertain significance |
| rs2501932844 | 14:23,635,596 | T/C | — | uncertain significance |
| rs1488274056 | 14:23,635,639 | C/T | — | uncertain significance |
| rs2048951263 | 14:23,635,723 | C/T | — | uncertain significance |
| rs145467931 | 14:23,641,535 | G/T | regulatory region variant | — |
| rs760406023 | 14:23,651,993 | C/G | — | uncertain significance |
| rs762716019 | 14:23,652,023 | A/G | — | uncertain significance |
| rs149980964 | 14:23,652,038 | G/A | — | benign |
| rs141772308 | 14:23,652,101 | C/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.