SLC25A1

Solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
Identifiers
Symbol(s)	SLC25A1; CTP; SLC20A3
External IDs	OMIM: 190315 MGI: 1345283 Homologene: 4362
Gene ontology Molecular Function: • transporter activity • binding • citrate transmembrane transporter activity Cellular Component: • mitochondrion • mitochondrial inner membrane • membrane • integral to membrane Biological Process: • transport • mitochondrial citrate transport
RNA expression pattern
250px More reference expression data
Orthologs
	Human	Mouse
Entrez	6576	13358
Ensembl	ENSG00000100075	ENSMUSG00000003528
Uniprot	P53007	na
Refseq	NM_005984 (mRNA) NP_005975 (protein)	NM_153150 (mRNA) NP_694790 (protein)
Location	Chr 22: 17.54 - 17.55 Mb	Chr 16: 17.84 - 17.84 Mb
Pubmed search	[1]	[2]

Solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1, also known as SLC25A1, is a human gene.

See also

• MeSH SLC25A1+protein,+human

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.
• Iacobazzi V, Lauria G, Palmieri F (1997). "Organization and sequence of the human gene for the mitochondrial citrate transport protein.". DNA Seq. 7 (3-4): 127-39. PMID 9254007.
• 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. PMID 8776594.
• Heisterkamp N, Mulder MP, Langeveld A, et al. (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.
• 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.

Template:Membrane-protein-stub This article incorporates text from the United States National Library of Medicine, which is in the public domain.