SLC15A4
solute carrier family 15 member 4
Summary
Enables several functions, including L-histidine transmembrane transporter activity; peptide:proton symporter activity; and peptidoglycan transmembrane transporter activity. Involved in dipeptide import across plasma membrane; peptidoglycan transport; and positive regulation of pattern recognition receptor signaling pathway. Located in endolysosome membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3765108 | 12:129,278,207 | T/C | 3 prime UTR variant | — |
| rs1955418654 | 12:129,278,748 | C/T | — | uncertain significance |
| rs369063412 | 12:129,278,769 | T/C | — | uncertain significance |
| rs372794236 | 12:129,278,781 | C/G | — | uncertain significance |
| rs1160800854 | 12:129,278,783 | C/G | — | uncertain significance |
| rs773611433 | 12:129,278,853 | G/A | — | uncertain significance |
| rs7308691 | 12:129,279,319 | T/A | regulatory region variant | — |
| rs773837932 | 12:129,283,873 | C/T | — | uncertain significance |
| rs1279162812 | 12:129,283,927 | T/C | — | uncertain significance |
| rs2541132592 | 12:129,283,956 | T/C | — | uncertain significance |
| rs1265345964 | 12:129,283,960 | G/T | — | uncertain significance |
| rs1187733419 | 12:129,285,428 | C/T | — | uncertain significance |
| rs767177677 | 12:129,285,471 | C/T | — | uncertain significance |
| rs12298615 | 12:129,286,756 | G/A | regulatory region variant | — |
| rs959989 | 12:129,292,708 | A/T | intron variant | — |
| rs1046446329 | 12:129,293,420 | T/C | — | likely benign |
| rs1424435148 | 12:129,294,538 | T/C | — | uncertain significance |
| rs771177586 | 12:129,294,556 | C/T | — | uncertain significance |
| rs11059928 | 12:129,296,103 | A/G | — | — |
| rs10847697 | 12:129,299,385 | G/A | synonymous variant | — |
| rs754716226 | 12:129,299,426 | C/T | — | uncertain significance |
| rs1379671934 | 12:129,299,483 | C/A | — | uncertain significance |
| rs1385374 | 12:129,300,694 | C/T | regulatory region variant | — |
| rs983492 | 12:129,306,121 | C/T | intron variant | — |
| rs1003148483 | 12:129,308,049 | T/G | — | uncertain significance |
| rs1454193418 | 12:129,308,050 | C/G | — | uncertain significance |
| rs1020860639 | 12:129,308,076 | A/G | — | uncertain significance |
| rs2541164669 | 12:129,308,121 | A/T | — | uncertain significance |
| rs771113231 | 12:129,308,181 | G/A | — | uncertain significance |
| rs746374738 | 12:129,308,185 | G/A | — | uncertain significance |
| rs770141231 | 12:129,308,187 | C/G | — | uncertain significance |
| rs2541165133 | 12:129,308,263 | C/T | — | uncertain significance |
| rs201649968 | 12:129,308,265 | C/T | — | uncertain significance |
| rs376263223 | 12:129,308,476 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.