SLC25A19

From Wikipedia, the free encyclopedia


Solute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19
Identifiers
Symbol(s) SLC25A19; DNC; MCPHA; MUP1
External IDs OMIM: 606521 MGI1914533 HomoloGene5982
Orthologs
Human Mouse
Entrez 60386 67283
Ensembl ENSG00000125454 ENSMUSG00000020744
Uniprot Q9HC21 Q80XJ6
Refseq NM_021734 (mRNA)
NP_068380 (protein)
NM_026071 (mRNA)
NP_080347 (protein)
Location Chr 17: 70.78 - 70.8 Mb Chr 11: 115.43 - 115.44 Mb
Pubmed search [1] [2]

Solute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19, also known as SLC25A19, is a human gene.[1]


[edit] See also

[edit] References

[edit] Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171-4. PMID 8125298. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149-56. PMID 9373149. 
  • Dolce V, Fiermonte G, Runswick MJ, et al. (2001). "The human mitochondrial deoxynucleotide carrier and its role in the toxicity of nucleoside antivirals.". Proc. Natl. Acad. Sci. U.S.A. 98 (5): 2284-8. doi:10.1073/pnas.031430998. PMID 11226231. 
  • Iacobazzi V, Ventura M, Fiermonte G, et al. (2001). "Genomic organization and mapping of the gene (SLC25A19) encoding the human mitochondrial deoxynucleotide carrier (DNC).". Cytogenet. Cell Genet. 93 (1-2): 40-2. PMID 11474176. 
  • Rosenberg MJ, Agarwala R, Bouffard G, et al. (2002). "Mutant deoxynucleotide carrier is associated with congenital microcephaly.". Nat. Genet. 32 (1): 175-9. doi:10.1038/ng948. PMID 12185364. 
  • 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. 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. PMID 15489334. 
  • Lam W, Chen C, Ruan S, et al. (2005). "Expression of deoxynucleotide carrier is not associated with the mitochondrial DNA depletion caused by anti-HIV dideoxynucleoside analogs and mitochondrial dNTP uptake.". Mol. Pharmacol. 67 (2): 408-16. doi:10.1124/mol.104.007120. PMID 15539640. 
  • Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 117-26. doi:10.1093/dnares/12.2.117. PMID 16303743. 
  • Lindhurst MJ, Fiermonte G, Song S, et al. (2006). "Knockout of Slc25a19 causes mitochondrial thiamine pyrophosphate depletion, embryonic lethality, CNS malformations, and anemia.". Proc. Natl. Acad. Sci. U.S.A. 103 (43): 15927-32. doi:10.1073/pnas.0607661103. PMID 17035501.