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SLC25A1: Wikis


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Solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
Symbols SLC25A1; CTP; SLC20A3
External IDs OMIM190315 MGI1345283 HomoloGene4362 GeneCards: SLC25A1 Gene
RNA expression pattern
PBB GE SLC25A1 210010 s at tn.png
More reference expression data
Species Human Mouse
Entrez 6576 13358
Ensembl ENSG00000100075 ENSMUSG00000003528
UniProt P53007 n/a
RefSeq (mRNA) NM_005984 NM_153150
RefSeq (protein) NP_005975 NP_694790
Location (UCSC) Chr 22:
17.54 - 17.55 Mb
Chr 16:
17.84 - 17.84 Mb
PubMed search [1] [2]

Tricarboxylate transport protein, mitochondrial is a protein that in humans is encoded by the SLC25A1 gene.[1][2][3]

See also


  1. ^ Heisterkamp N, Mulder MP, Langeveld A, ten Hoeve J, Wang Z, Roe BA, Groffen J (Aug 1996). "Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region". Genomics 29 (2): 451-6. PMID 8666394.  
  2. ^ Iacobazzi V, Lauria G, Palmieri F (Sep 1997). "Organization and sequence of the human gene for the mitochondrial citrate transport protein". DNA Seq 7 (3-4): 127-39. PMID 9254007.  
  3. ^ "Entrez Gene: SLC25A1 solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1".  

Further reading

  • Ewing RM, Chu P, Elisma F, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry.". Mol. Syst. Biol. 3: 89. doi:10.1038/msb4100134. PMID 17353931.  
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.  
  • 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.  
  • 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.  
  • Gong W, Emanuel BS, Collins J, et al. (1996). "A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.". Hum. Mol. Genet. 5 (6): 789–800. doi:10.1093/hmg/5.6.789. PMID 8776594.  
  • Goldmuntz E, Wang Z, Roe BA, Budarf ML (1997). "Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region.". Genomics 33 (2): 271–6. doi:10.1006/geno.1996.0191. PMID 8660975.  

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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