| ID | Sequence | Length | GC content |
|---|---|---|---|
| CUUUUUUGCGCCGGCUGUGACAAGCGCUGCGGCAUUUGUCCCCGCGACA… | 721 nt | 0.6685 | |
| CUUUUUUGCGCCGGCUGUGACAAGCGCUGCGGCAUUUGUCCCCGCGACA… | 700 nt | 0.6700 |
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]
A study in Sprague-Dawley rats demonstrated that the gene CHCHD10 was among the top five differentially expressed genes upregulated in the spinal cord at 3 and 7 days post-tibial fracture compared to a 0-day control [Deng et al. DOI:10.1038/s41598-025-17561-6].