SLC15A2
solute carrier family 15 member 2
Pharmacogene
Summary
The mammalian kidney expresses a proton-coupled peptide transporter that is responsible for the absorption of small peptides, as well as beta-lactam antibiotics and other peptide-like drugs, from the tubular filtrate. This transporter, SLC15A2, belongs to the same gene family as SLC15A1 (MIM 600544), the proton-coupled peptide transporter found in the small intestine (Liu et al, 1995 [PubMed 7756356]).[supplied by OMIM, Feb 2011]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2472657785 | 3:121,613,337 | A/G | — | uncertain significance |
| rs773729056 | 3:121,615,259 | T/C | — | uncertain significance |
| rs192955628 | 3:121,615,272 | A/G | — | uncertain significance |
| rs2472660864 | 3:121,615,284 | T/C | — | uncertain significance |
| rs576461255 | 3:121,615,287 | C/G | — | uncertain significance |
| rs752943810 | 3:121,616,261 | T/A | — | uncertain significance |
| rs773867721 | 3:121,616,358 | C/T | — | uncertain significance |
| rs9842387 | 3:121,616,995 | A/C | — | — |
| rs9815756 | 3:121,618,984 | G/T | intron variant | — |
| rs2877569 | 3:121,621,382 | A/G | intron variant | — |
| rs9713657 | 3:121,624,741 | G/C | intron variant | — |
| rs9714033 | 3:121,624,742 | T/A | — | — |
| rs7635449 | 3:121,626,634 | T/A | — | — |
| rs9289182 | 3:121,628,360 | A/C | — | — |
| rs896881989 | 3:121,630,447 | A/G | — | uncertain significance |
| rs866929 | 3:121,632,507 | G/A | intron variant | — |
| rs2472698639 | 3:121,634,504 | T/C | — | uncertain significance |
| rs769832128 | 3:121,634,517 | G/T | — | uncertain significance |
| rs2689282 | 3:121,637,803 | C/T | downstream gene variant | — |
| rs9822474 | 3:121,637,966 | A/G | regulatory region variant | — |
| rs9871534 | 3:121,640,177 | G/C | — | — |
| rs9816071 | 3:121,640,318 | T/G | — | — |
| rs9816215 | 3:121,640,426 | T/A | — | — |
| rs915334077 | 3:121,641,142 | G/A | — | uncertain significance |
| rs1178760016 | 3:121,641,624 | T/A | — | uncertain significance |
| rs1198713622 | 3:121,641,917 | A/C | — | uncertain significance |
| rs201759568 | 3:121,642,070 | G/A | — | uncertain significance |
| rs866764019 | 3:121,642,076 | G/A | — | uncertain significance |
| rs2472712182 | 3:121,642,098 | G/C | — | uncertain significance |
| rs2293614 | 3:121,642,246 | C/G | — | — |
| rs2472713752 | 3:121,643,202 | T/C | — | uncertain significance |
| rs2257212 | 3:121,643,804 | C/G | missense variant | — |
| rs766336700 | 3:121,643,826 | C/T | — | uncertain significance |
| rs2472715091 | 3:121,643,834 | G/A | — | uncertain significance |
| rs2250065 | 3:121,644,029 | G/A | — | — |
| rs2250067 | 3:121,644,030 | C/T | regulatory region variant | — |
| rs11707541 | 3:121,644,529 | C/A | upstream gene variant | — |
| rs9870245 | 3:121,645,438 | G/A | upstream gene variant | — |
| rs1143671 | 3:121,647,286 | C/A | missense variant | — |
| rs1218053874 | 3:121,647,331 | G/A | — | uncertain significance |
| rs144786366 | 3:121,647,396 | C/T | — | benign |
| rs748018463 | 3:121,647,881 | A/G | — | uncertain significance |
| rs1143672 | 3:121,648,168 | G/A | missense variant | — |
| rs76469580 | 3:121,648,175 | C/A | — | likely benign |
| rs758687526 | 3:121,650,550 | T/G | — | uncertain significance |
| rs75557865 | 3:121,652,141 | G/A | intron variant | — |
| rs9868185 | 3:121,657,593 | A/T | — | — |
| rs1143668 | 3:121,658,260 | C/T | — | likely benign |
| rs370025673 | 3:121,658,304 | A/G | — | uncertain significance |
| rs760188635 | 3:121,659,276 | A/G | — | uncertain significance |
| rs368922326 | 3:121,659,280 | T/C | — | uncertain significance |
| rs745365197 | 3:121,659,300 | G/A | — | uncertain significance |
| rs1334433008 | 3:121,659,688 | T/C | — | uncertain significance |
| rs138745887 | 3:121,659,777 | C/T | missense variant | — |
| rs4285028 | 3:121,660,664 | A/G | — | — |
| rs9856253 | 3:121,661,910 | C/G | — | — |
| rs1480057696 | 3:121,911,667 | G/A | splice donor variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.