SLC25A1
From Wikipedia, the free encyclopedia
Solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
|
||||||||||||||
Identifiers | ||||||||||||||
Symbol(s) | SLC25A1; CTP; SLC20A3 | |||||||||||||
External IDs | OMIM: 190315 MGI: 1345283 HomoloGene: 4362 | |||||||||||||
|
||||||||||||||
RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 6576 | 13358 | ||||||||||||
Ensembl | ENSG00000100075 | ENSMUSG00000003528 | ||||||||||||
Uniprot | P53007 | n/a | ||||||||||||
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.[1]
[edit] See also
[edit] References
[edit] 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: . 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: . 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: . 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: . 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: . PMID 8660975.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.