This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.[provided by RefSeq, May 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A15-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A15-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.[provided by RefSeq, May 2009]
Gene Symbol : SLC25A15
Gene Name : Solute carrier family 25 member 15
Chromosome : CHR 13: 407,894,10-408,124,59
Locus : 13q14.11
Alt. Genes : LRPPRC
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