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SLC25A12
Calcium-binding mitochondrial carrier protein Aralar1 is a protein that in humans is encoded by the SLC25A12 gene.[1][2][3][4]
See also
References
- ^ 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. PMID 9722566. doi:10.1074/jbc.273.36.23327.
- ^ 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. PMID 10702666. doi:10.1159/000015465.
- ^ 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. PMC 125626. PMID 11566871. doi:10.1093/emboj/20.18.5060.
- ^ "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. PMID 10369257. doi:10.1038/9667.
- 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. doi:10.1159/000015595.
- 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. PMC 139241. PMID 12477932. doi:10.1073/pnas.242603899.
- 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. PMID 14702039. doi:10.1038/ng1285.
- 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. doi:10.1176/appi.ajp.161.4.662.
- 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. PMID 15494407. doi:10.1074/jbc.M409303200.
- 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. PMID 16648338. doi:10.1176/appi.ajp.163.5.929.
- 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. PMC 1847948. PMID 17353931. doi:10.1038/msb4100134.
- 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. PMID 17693006. doi:10.1016/j.pnpbp.2007.07.010.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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