SLC13A2

An Error has occured retrieving Wikidata item for infobox SLC13A2‏ (Solute carrier family 13 member 2) هوَ بروتين يُشَفر بواسطة جين SLC13A2 في الإنسان.^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ Mann SS، Hart TC، Pettenati MJ، von Kap-herr C، Holmes RP (يونيو 1999). "Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2 alias NaDC-1) to human chromosome region 17p11.1→q11.1 by radiation hybrid mapping and fluorescence in situ hybridization". Cytogenet Cell Genet. ج. 84 ع. 1–2: 89–90. DOI:10.1159/000015222. PMID:10343111.
^ Pajor AM (ديسمبر 1996). "Molecular cloning and functional expression of a sodium-dicarboxylate cotransporter from human kidney". Am J Physiol. ج. 270 ع. 4 Pt 2: F642–8. PMID:8967342.
^ "Entrez Gene: SLC13A2 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2". مؤرشف من الأصل في 2010-12-05.

قراءة متعمقة

Inoue K، Zhuang L، Ganapathy V (2003). "Human Na+ -coupled citrate transporter: primary structure, genomic organization, and transport function". Biochem. Biophys. Res. Commun. ج. 299 ع. 3: 465–71. DOI:10.1016/S0006-291X(02)02669-4. PMID:12445824.
Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
Bai X، Chen X، Fen Z، وآخرون (2005). "Expression of EGFP/SDCT1 fusion protein, subcellular localization signal analysis, tissue distribution and electrophysiological function study". Sci. China, C, Life Sci. ج. 47 ع. 6: 530–9. DOI:10.1360/03yc0044. PMID:15620109.
Pajor AM، Randolph KM (2005). "Conformationally sensitive residues in extracellular loop 5 of the Na+/dicarboxylate co-transporter". J. Biol. Chem. ج. 280 ع. 19: 18728–35. DOI:10.1074/jbc.M501265200. PMC:1224748. PMID:15774465.
Okamoto N، Aruga S، Matsuzaki S، وآخرون (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. ج. 14 ع. 4: 344–9. DOI:10.1111/j.1442-2042.2007.01554.x. PMID:17470169.

هذه بذرة مقالة عن جين على كروموسوم 17 بحاجة للتوسيع. فضلًا شارك في تحريرها.

[pmid10343111-1] Mann SS، Hart TC، Pettenati MJ، von Kap-herr C، Holmes RP (يونيو 1999). "Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2 alias NaDC-1) to human chromosome region 17p11.1→q11.1 by radiation hybrid mapping and fluorescence in situ hybridization". Cytogenet Cell Genet. ج. 84 ع. 1–2: 89–90. DOI:10.1159/000015222. PMID:10343111.

[pmid8967342-2] Pajor AM (ديسمبر 1996). "Molecular cloning and functional expression of a sodium-dicarboxylate cotransporter from human kidney". Am J Physiol. ج. 270 ع. 4 Pt 2: F642–8. PMID:8967342.

[entrez-3] "Entrez Gene: SLC13A2 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2". مؤرشف من الأصل في 2010-12-05.

[1]

[2]

[3]