This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A12-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A12-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A12-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A12-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A12-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]
Gene Symbol : SLC25A12
Gene Name : Solute carrier family 25 member 12
Chromosome : CHR 2: 171,894,305-171,783,404
Locus : 2q31.1
Alt. Genes : OPTN
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