SLC25A12
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Calcium-binding mitochondrial carrier protein Aralar1 is a protein that in humans is encoded by the SLC25A12 gene.[4][5][6][7]
See also
References
- ↑ "Diseases that are genetically associated with SLC25A12 view/edit references on wikidata".
- ↑ "Human PubMed Reference:".
- ↑ "Mouse PubMed Reference:".
- ↑ del Arco A; Satrustegui J (Oct 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. doi:10.1074/jbc.273.36.23327. PMID 9722566.
- ↑ Crackower MA; Sinasac DS; Lee JR; Herbrick JA; Tsui LC; Scherer SW (Apr 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. doi:10.1159/000015465. PMID 10702666.
- ↑ Palmieri L; Pardo B; Lasorsa FM; del Arco A; Kobayashi K; Iijima M; Runswick MJ; Walker JE; Saheki T; Satrustegui J; Palmieri F (Sep 2001). "Citrin and aralar1 are Ca2+-stimulated aspartate/glutamate transporters in mitochondria". EMBO J. 20 (18): 5060–9. doi:10.1093/emboj/20.18.5060. PMC 125626. PMID 11566871.
- ↑ "Entrez Gene: SLC25A12 solute carrier family 25 (mitochondrial carrier, Aralar), member 12".
Further reading
- 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:10.1038/9667. PMID 10369257.
- 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. doi:10.1159/000015595. PMID 10965105.
- 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. PMC 139241. 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.
- 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. doi:10.1176/appi.ajp.161.4.662. 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:10.1074/jbc.M409303200. 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:10.1176/appi.ajp.163.5.929. 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 (1): 89. doi:10.1038/msb4100134. PMC 1847948. 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:10.1016/j.pnpbp.2007.07.010. PMID 17693006.
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