This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A4-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A4-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A4-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A4-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A4-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]
Gene Symbol : SLC25A4
Gene Name : Solute carrier family 25 member 4
Chromosome : CHR 4: 185,143,262-185,150,383
Locus : 4q35.1
Alt. Genes : OPTN
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