This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A1-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A1-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A1-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A1-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
Gene Symbol : SLC25A1
Gene Name : Solute carrier family 25 member 1
Chromosome : CHR 22: 191,788,62-191,755,74
Locus : 22q11.21
Alt. Genes : KIF20A
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