This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19. [provided by RefSeq, Aug 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CHCHD10-20-RE | 20 (40 μL) | 200 μL |  |
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| CHCHD10-20-OR | 20 (40 μL) | 200 μL |  |
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| CHCHD10-20-GO | 20 (40 μL) | 200 μL |  |
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| CHCHD10-20-GR | 20 (40 μL) | 200 μL |  |
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| CHCHD10-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19. [provided by RefSeq, Aug 2014]
Gene Symbol : CHCHD10
Gene Name : Coiled-coil-helix-coiled-coil-helix domain containing 10
Chromosome : CHR 22: 237,679,71-237,658,33
Locus : 22q11.23
Alt. Genes : CEBPZ
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