solute carrier family 22 member 18 (SLC22A18, organic cation transporter-like protein 2, imprinted multi-membrane spanning polyspecific transporter-related protein 1, efflux transporter-like protein, tumor-suppressing subchromosomal transferable fragment candidate gene protein 5, tumor-suppressing STF cDNA 5 protein, Beckwith-Wiedemann syndrome chromosome region 1 candidate protein A, p45-Beckwith-Wiedemann region 1 A, p45-BWR1A, solute carrier family 22 member 1-like, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5)
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Function
- transporter of organic cations via proton efflux antiport (putative)
- role in transport of chloroquine & quinidine-related compounds in kidney (putative)
- interacts with RNF167
Structure
- belongs to the major facilitator superfamily, organic cation transporter family
Compartment
- apical cell membrane
- localized at the apical membrane surface of renal proximal tubules
Expression
- expressed in adult & fetal kidney & liver,& adult colon > heart, brain & lung
- expressed in fetal renal proximal tubules (at protein level)
Pathology
- defects in SLC22A18 are associated with
- defects in SLC22A18 are the cause of rhabdomyosarcoma type 1