CHCHD10
protein-coding gene in the species Homo sapiens
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Summary
CHCHD10 is a gene[1]. CHCHD10 is known by 8 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 27885[4]
- Genomic start: 23765834[5], 24108021[6]
- Genomic end: 24110630[7], 23767972[8]
- Ortholog: Chchd10[9]
- Encodes: Coiled-coil-helix-coiled-coil-helix domain containing 10[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 22[12]
- Genetic association: FTDALS2[13], autosomal dominant mitochondrial myopathy with exercise intolerance[14], Jokela type spinal muscular atrophy[15], amyotrophic lateral sclerosis and frontotemporal dementia[16]
- Strand orientation: reverse strand[17]
- Exact match: http://identifiers.org/ncbigene/400916[18]
- Cytogenetic location: 22q11.23[19]
- Expressed in: apex of heart[20], left ventricle[21], muscle of thigh[22], right auricle of heart[23], gastrocnemius muscle[24], skeletal muscle tissue[25], mucosa of transverse colon[26], primary visual cortex[27], right lobe of liver[28], human kidney[29]