This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A13-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A13-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A13-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A13-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A13-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Gene Symbol : SLC25A13
Gene Name : Solute carrier family 25 member 13
Chromosome : CHR 7: 963,221,46-961,202,19
Locus : 7q21.3
Alt. Genes : LRPPRC
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