This nuclear gene encodes a mitochondrial matrix protein that appears to contribute to peptide chain termination in the mitochondrial translation machinery. Two different 1 bp deletions (resulting in the same premature stop codon)result in decreased mitochondrial translation, decreased levels of oxidative phosphorylation complexes and encepthalomyopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| C12ORF65-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| C12ORF65-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| C12ORF65-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| C12ORF65-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| C12ORF65-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
This nuclear gene encodes a mitochondrial matrix protein that appears to contribute to peptide chain termination in the mitochondrial translation machinery. Two different 1 bp deletions (resulting in the same premature stop codon)result in decreased mitochondrial translation, decreased levels of oxidative phosphorylation complexes and encepthalomyopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
Gene Symbol : C12ORF65
Gene Name : Chromosome 12 open reading frame 65
Chromosome : CHR 12: 123,233,296-123,257,958
Locus : 12q24.31
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.