This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| AFG3L2-20-RE | 20 (40 μL) | 200 μL |  |
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| AFG3L2-20-OR | 20 (40 μL) | 200 μL |  |
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| AFG3L2-20-GO | 20 (40 μL) | 200 μL |  |
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| AFG3L2-20-GR | 20 (40 μL) | 200 μL |  |
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| AFG3L2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]
Gene Symbol : AFG3L2
Gene Name : AFG3 like matrix AAA peptidase subunit 2
Chromosome : CHR 18: 123,773,08-123,289,43
Locus : 18p11.21
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