The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2. [provided by RefSeq, Mar 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PMPCA-20-RE | 20 (40 μL) | 200 μL |  |
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| PMPCA-20-OR | 20 (40 μL) | 200 μL |  |
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| PMPCA-20-GO | 20 (40 μL) | 200 μL |  |
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| PMPCA-20-GR | 20 (40 μL) | 200 μL |  |
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| PMPCA-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2. [provided by RefSeq, Mar 2016]
Gene Symbol : PMPCA
Gene Name : Peptidase, mitochondrial processing alpha subunit
Chromosome : CHR 9: 136,410,572-136,423,760
Locus : 9q34.3
Alt. Genes : HIPK3
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