Citrin
From Wikipedia, the free encyclopedia
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solute carrier family 25, member 13 (citrin)
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| Identifiers | |
| Symbol | SLC25A13 |
| Alt. Symbols | CTLN2 |
| Entrez | 10165 |
| HUGO | 10983 |
| OMIM | 603859 |
| RefSeq | NM_014251 |
| UniProt | Q9UJS0 |
| Other data | |
| Locus | Chr. 7 q21.3 |
Citrin also known as solute carrier family 25, member 13 (citrin) or SLC25A13 is a protein associated with type II citrullinemia.[1][2][3]
[edit] See also
[edit] References
- ^ Saheki T, Kobayashi K (2002). "Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)". J. Hum. Genet. 47 (7): 333–41. doi:. PMID 12111366.
- ^ Saheki T, Kobayashi K, Iijima M, Nishi I, Yasuda T, Yamaguchi N, Gao HZ, Jalil MA, Begum L, Li MX (2002). "Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiency". Metab Brain Dis 17 (4): 335–46. PMID 12602510.
- ^ Saheki T, Kobayashi K, Iijima M, Horiuchi M, Begum L, Jalil MA, Li MX, Lu YB, Ushikai M, Tabata A, Moriyama M, Hsiao KJ, Yang Y (2004). "Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle". Mol. Genet. Metab. 81 Suppl 1: S20–6. doi:. PMID 15050970.

