SLC25A12
From Wikipedia, the free encyclopedia
Solute carrier family 25 (mitochondrial carrier, Aralar), member 12
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Identifiers | ||||||||||||||
Symbol(s) | SLC25A12; ARALAR; ARALAR1 | |||||||||||||
External IDs | OMIM: 603667 MGI: 1926080 HomoloGene: 48235 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 8604 | 78830 | ||||||||||||
Ensembl | ENSG00000115840 | ENSMUSG00000027010 | ||||||||||||
Uniprot | O75746 | Q8BH59 | ||||||||||||
Refseq | NM_003705 (mRNA) NP_003696 (protein) |
NM_172436 (mRNA) NP_766024 (protein) |
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Location | Chr 2: 172.35 - 172.46 Mb | Chr 2: 71.07 - 71.17 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Solute carrier family 25 (mitochondrial carrier, Aralar), member 12, also known as SLC25A12, is a human gene.[1]
[edit] See also
[edit] References
[edit] Further reading
- del Arco A, Satrústegui J (1998). "Molecular cloning of Aralar, a new member of the mitochondrial carrier superfamily that binds calcium and is present in human muscle and brain.". J. Biol. Chem. 273 (36): 23327–34. PMID 9722566.
- Kobayashi K, Sinasac DS, Iijima M, et al. (1999). "The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.". Nat. Genet. 22 (2): 159–63. doi: . PMID 10369257.
- Crackower MA, Sinasac DS, Lee JR, et al. (2000). "Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24.". Cytogenet. Cell Genet. 87 (3-4): 197–8. PMID 10702666.
- Sanz R, del Arco A, Ayuso C, et al. (2000). "Assignment of the calcium-binding mitochondrial carrier Aralar1 gene (SLC25A12) to human chromosome band 2q31 by in situ hybridization.". Cytogenet. Cell Genet. 89 (3-4): 143–4. PMID 10965105.
- Palmieri L, Pardo B, Lasorsa FM, et al. (2001). "Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria.". EMBO J. 20 (18): 5060–9. doi: . PMID 11566871.
- 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.
- 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: . PMID 14702039.
- Ramoz N, Reichert JG, Smith CJ, et al. (2004). "Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.". The American journal of psychiatry 161 (4): 662–9. PMID 15056512.
- Rubi B, del Arco A, Bartley C, et al. (2005). "The malate-aspartate NADH shuttle member Aralar1 determines glucose metabolic fate, mitochondrial activity, and insulin secretion in beta cells.". J. Biol. Chem. 279 (53): 55659–66. doi: . PMID 15494407.
- Rabionet R, McCauley JL, Jaworski JM, et al. (2006). "Lack of association between autism and SLC25A12.". The American journal of psychiatry 163 (5): 929–31. doi: . PMID 16648338.
- 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.
- Hong CJ, Liou YJ, Liao DL, et al. (2007). "Association study of polymorphisms in the mitochondrial aspartate/glutamate carrier SLC25A12 (aralar) gene with schizophrenia.". Prog. Neuropsychopharmacol. Biol. Psychiatry 31 (7): 1510–3. doi: . PMID 17693006.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.