| Gene Name | CHCHD10 |
|
| Specie | Homo sapiens | |
| Full Name | coiled-coil-helix-coiled-coil-helix domain containing 10 | |
| Also known as | C22orf16|FTDALS2|IMMD|MIX17A|N27C7-4|SMAJ | |
| Coordinate | chr22:23765834-23767972 | |
| Strand | - | |
| Gene summary | 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] |
| Retroname | Coord | Strand | Genomic Region | ENSG | |
|---|---|---|---|---|---|
| CHCHD10P2 | chr19:10216988-10217320 | - |
Intergenic |
N/A | UCSC |
| CHCHD10P1 | chr7:38311307-38311970 | + |
Intergenic |
ENSG00000231916 | UCSC |
| >NM_213720.3 |
| CTTTTTTGCGCCGGCTGTGACAAGCGCTGCGGCATTTGTCCCCGCGACAGCACCGCTGCCGCCGTCTCTAAGGTCGCCCGGGTCCCACCGCCGCCACCATGCCTCGGGGAAGCCGCAGCGCGGCCTCCCGGCCAGCCAGCCGCCCAGCCGCGCCCTCTGCCCACCCGCCCGCGCACCCACCGCCCTCGGCAGCCGCCCCAGCCCCCGCCCCTTCGGGCCAGCCGGGGCTCATGGCTCAGATGGCGACCACGGCCGCAGGGGTAGCCGTGGGCTCGGCTGTGGGACACGTCATGGGCAGCGCCCTGACCGGAGCCTTCAGCGGGGGGAGCTCGGAGCCCTCCCAGCCTGCTGTCCAGCAGGCCCCCACCCCCGCTGCCCCCCAGCCCCTGCAGATGGGGCCCTGCGCCTACGAGATCAGGCAGTTCCTGGACTGTTCCACCACTCAGAGTGACCTGTCCCTGTGTGAGGGCTTCAGCGAGGCCCTGAAGCAGTGCAAGTACTACCATGGTCTGAGCTCCCTGCCCTGAAGAGGTCGGTGCAGACTCGGGGGCCAGTCCTGCACCCACCTCTACCCCTCGCCGACAGCCAGACCACAACACCAGATTGTACCCAGATAGCTGGGATTGGAAGTGAGGAGGTTTCTCACCCCACAGATAACCCAAGACACAAATGTGCAATTAAAAGTTTATTTTAGACCACA |