This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jul 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A22-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A22-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A22-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A22-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A22-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jul 2010]
Gene Symbol : SLC25A22
Gene Name : Solute carrier family 25 member 22
Chromosome : CHR 11: 798,268-790,474
Locus : 11p15.5
Alt. Genes : CEBPZ
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