SLC25A39: Difference between revisions
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'''Solute carrier family 25 member 39''' is a [[protein]] that in humans is encoded by the ''SLC25A39'' [[gene]].<ref name="pmid16949250">{{cite journal | vauthors = Haitina T, Lindblom J, Renstrom T, Fredriksson R | title = Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system | journal = Genomics | volume = 88 | issue = 6 | pages = 779–90 |date=Nov 2006 | pmid = 16949250 | pmc = | doi = 10.1016/j.ygeno.2006.06.016 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC25A39 solute carrier family 25, member 39| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51629| accessdate = }}</ref> | '''Solute carrier family 25 member 39''' is a [[protein]] that in humans is encoded by the ''SLC25A39'' [[gene]].<ref name="pmid16949250">{{cite journal | vauthors = Haitina T, Lindblom J, Renstrom T, Fredriksson R | title = Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system | journal = Genomics | volume = 88 | issue = 6 | pages = 779–90 |date=Nov 2006 | pmid = 16949250 | pmc = | doi = 10.1016/j.ygeno.2006.06.016 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC25A39 solute carrier family 25, member 39| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51629| accessdate = }}</ref> | ||
Latest revision as of 18:54, 20 February 2018
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Solute carrier family 25 member 39 is a protein that in humans is encoded by the SLC25A39 gene.[1][2]
See also
- SLC25A39+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
References
- ↑ Haitina T, Lindblom J, Renstrom T, Fredriksson R (Nov 2006). "Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system". Genomics. 88 (6): 779–90. doi:10.1016/j.ygeno.2006.06.016. PMID 16949250.
- ↑ "Entrez Gene: SLC25A39 solute carrier family 25, member 39".
Further reading
- 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.
- 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.
- 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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
- Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
- Yu XX, Lewin DA, Zhong A, et al. (2001). "Overexpression of the human 2-oxoglutarate carrier lowers mitochondrial membrane potential in HEK-293 cells: contrast with the unique cold-induced mitochondrial carrier CGI-69". Biochem. J. 353 (Pt 2): 369–75. doi:10.1042/0264-6021:3530369. PMC 1221580. PMID 11139402.
- Lai CH, Chou CY, Ch'ang LY, et al. (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Res. 10 (5): 703–13. doi:10.1101/gr.10.5.703. PMC 310876. PMID 10810093.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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