SLC38A9
solute carrier family 38 member 9
Summary
Enables several functions, including L-amino acid transmembrane transporter activity; cholesterol binding activity; and guanyl-nucleotide exchange factor activity. Involved in carboxylic acid transport; cellular response to amino acid stimulus; and positive regulation of TORC1 signaling. Located in Ragulator complex; late endosome; and lysosomal membrane. Part of FNIP-folliculin RagC/D GAP. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374737727 | 5:54,922,354 | C/T | — | uncertain significance |
| rs1742443396 | 5:54,922,369 | T/C | — | uncertain significance |
| rs773927493 | 5:54,922,375 | C/T | — | likely benign |
| rs1017198374 | 5:54,922,429 | T/C | — | uncertain significance |
| rs774465789 | 5:54,929,592 | T/C | — | likely benign |
| rs748225255 | 5:54,929,598 | C/T | — | uncertain significance |
| rs761335670 | 5:54,929,610 | C/T | — | uncertain significance |
| rs184922428 | 5:54,929,625 | G/A | — | uncertain significance |
| rs149447829 | 5:54,929,694 | A/G | — | uncertain significance |
| rs13156231 | 5:54,930,251 | T/A | — | — |
| rs765046146 | 5:54,931,445 | G/A | — | uncertain significance |
| rs2478884079 | 5:54,931,460 | A/C | — | uncertain significance |
| rs187154786 | 5:54,941,697 | T/A | — | benign |
| rs7704138 | 5:54,944,262 | C/A | — | — |
| rs771145523 | 5:54,945,050 | C/T | — | uncertain significance |
| rs2530775703 | 5:54,948,446 | G/C | — | uncertain significance |
| rs368805124 | 5:54,948,539 | C/G | — | uncertain significance |
| rs9687085 | 5:54,948,811 | C/G | — | — |
| rs920961719 | 5:54,952,560 | G/A | — | uncertain significance |
| rs1301462264 | 5:54,952,568 | T/C | — | uncertain significance |
| rs145115923 | 5:54,960,577 | A/G | — | uncertain significance |
| rs201069974 | 5:54,965,068 | G/A | — | uncertain significance |
| rs994530153 | 5:54,965,095 | A/G | — | uncertain significance |
| rs1750919459 | 5:54,965,130 | A/G | — | uncertain significance |
| rs2531282804 | 5:54,965,410 | A/G | — | uncertain significance |
| rs1488636361 | 5:54,965,594 | T/A | — | uncertain significance |
| rs199794672 | 5:54,965,611 | C/T | — | uncertain significance |
| rs759802643 | 5:54,968,419 | C/T | — | uncertain significance |
| rs968815885 | 5:54,968,501 | T/C | — | uncertain significance |
| rs563588997 | 5:54,976,969 | G/A | — | — |
| rs1179471099 | 5:54,984,401 | G/T | — | — |
| rs770064253 | 5:54,987,018 | G/A | — | likely benign |
| rs6864532 | 5:54,992,679 | G/C | — | — |
| rs144207377 | 5:54,993,761 | C/T | — | uncertain significance |
| rs11958779 | 5:55,001,899 | G/A | intron variant | — |
| rs67820074 | 5:55,009,278 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.