SLC22A25
      
Solute carrier family 22 member 25 (SLC22A25), also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC22A25 gene.[3][4]
References
Further reading
- Eraly SA; Monte JC; Nigam SK (2004). "Novel slc22 transporter homologs in fly, worm, and human clarify the phylogeny of organic anion and cation transporters.". Physiol. Genomics. 18 (1): 12–24. doi:10.1152/physiolgenomics.00014.2004. PMID 15054140. 
- Strausberg RL, Feingold EA, Grouse LH,  et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241 . PMID 12477932. . PMID 12477932.
- Zaïr ZM; Eloranta JJ; Stieger B; Kullak-Ublick GA (2008). "Pharmacogenetics of OATP (SLC21/SLCO), OAT and OCT (SLC22) and PEPT (SLC15) transporters in the intestine, liver and kidney.". Pharmacogenomics. 9 (5): 597–624. doi:10.2217/14622416.9.5.597. PMID 18466105. 
- Ota T, Suzuki Y, Nishikawa T,  et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039. 
 
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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 |  |  |  | | SLC11–20 | 
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 proton coupled metal ion transporter
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 human Na+-sulfate/carboxylate cotransporter
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 proton oligopeptide cotransporter
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 monocarboxylate transporter
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 |  |  |  | | SLC21–30 | 
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 Na+-dependent ascorbic acid transporter
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 multifunctional anion exchanger
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 Na+-coupled nucleoside transport (SLC28A1
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 facilitative nucleoside transporter
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 |  |  |  | | SLC31–40 | 
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 type II Na+-phosphate cotransporter
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 nucleoside-sugar transporter
 SLC35E1 SLC35E2 SLC35E3 SLC35E4
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 proton-coupled amino-acid transporter
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 sugar-phosphate/phosphate exchanger
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 System A & N, sodium-coupled neutral amino-acid transporter
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 basolateral iron transporter
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 Na+-independent, system-L like amino-acid transporter
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 Putative sugar transporter
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| see also solute carrier disorders |