Solute carrier family 13 member 2 is a protein that is encoded in humans by the SLC13A2 gene.[5][6][7]
References
Further reading
- Inoue K, Zhuang L, Ganapathy V (2003). "Human Na+ -coupled citrate transporter: primary structure, genomic organization, and transport function". Biochem. Biophys. Res. Commun. 299 (3): 465–71. doi:10.1016/S0006-291X(02)02669-4. PMID 12445824.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- 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.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Bai X, Chen X, Fen Z, et al. (2005). "Expression of EGFP/SDCT1 fusion protein, subcellular localization signal analysis, tissue distribution and electrophysiological function study". Science in China Series C: Life Sciences. 47 (6): 530–9. doi:10.1360/03yc0044. PMID 15620109. S2CID 36487757.
- Pajor AM, Randolph KM (2005). "Conformationally sensitive residues in extracellular loop 5 of the Na+/dicarboxylate co-transporter". J. Biol. Chem. 280 (19): 18728–35. doi:10.1074/jbc.M501265200. PMC 1224748. PMID 15774465.
- Okamoto N, Aruga S, Matsuzaki S, et al. (2007). "Associations between renal sodium-citrate cotransporter (hNaDC-1) gene polymorphism and urinary citrate excretion in recurrent renal calcium stone formers and normal controls". Int. J. Urol. 14 (4): 344–9. doi:10.1111/j.1442-2042.2007.01554.x. PMID 17470169. S2CID 41274929.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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By group |
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SLC1–10 |
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(1): | |
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(2): | |
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(3): | |
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(4): | |
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(5): | |
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(6): | |
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(7): | |
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(8): | |
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(9): | |
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(10): | |
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| SLC11–20 |
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(11): |
- proton coupled metal ion transporter
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(12): | |
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(13): |
- human Na+-sulfate/carboxylate cotransporter
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(14): | |
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(15): |
- proton oligopeptide cotransporter
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(16): |
- monocarboxylate transporter
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(17): | |
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(18): | |
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(19): | |
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(20): | |
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| SLC21–30 |
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(21): | |
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(22): | |
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(23): |
- Na+-dependent ascorbic acid transporter
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(24): | |
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(25): | |
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(26): |
- multifunctional anion exchanger
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(27): | |
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(28): |
- Na+-coupled nucleoside transport (SLC28A1
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(29): |
- facilitative nucleoside transporter
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(30): | |
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| SLC31–40 |
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(31): | |
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(32): | |
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(33): | |
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(34): |
- type II Na+-phosphate cotransporter
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(35): |
- nucleoside-sugar transporter
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-
-
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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(36): | |
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(37): |
- sugar-phosphate/phosphate exchanger
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(38): |
- System A & N, sodium-coupled neutral amino-acid transporter
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(39): | |
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(40): |
- basolateral iron transporter
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| SLC41–48 |
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(41): | |
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(42): | |
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(43): |
- Na+-independent, system-L like amino-acid transporter
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(44): | |
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(45): |
- Putative sugar transporter
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(46): | |
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(47): | |
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(48): | |
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see also solute carrier disorders |