The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| OPA1-20-RE | 20 (40 μL) | 200 μL |  |
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| OPA1-20-OR | 20 (40 μL) | 200 μL |  |
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| OPA1-20-GO | 20 (40 μL) | 200 μL |  |
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| OPA1-20-GR | 20 (40 μL) | 200 μL |  |
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| OPA1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]
Gene Symbol : OPA1
Gene Name : OPA1, mitochondrial dynamin like GTPase
Chromosome : CHR 3: 193,593,143-193,697,810
Locus : 3q29
Alt. Genes : FEM1B
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