Chchd10 Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
Chchd10 Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
| CHCHD10 Gene | |
|---|---|
| Gene Symbol | CHCHD10 |
| Full Name | Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 10 |
| Chromosomal Location | 22q11.23 |
| NCBI Gene ID | 400916 |
| OMIM | 614643 |
| Ensembl ID | ENSG00000151353 |
| UniProt ID | Q8N5L4 |
CHCHD10 encodes a mitochondrial protein involved in:
| Disease | Inheritance | Mechanism |
|---|---|---|
| Amyotrophic Lateral Sclerosis (ALS) | Autosomal dominant | Mitochondrial dysfunction, aggregate formation |
| Frontotemporal Dementia (FTD) | Autosomal dominant | Mitochondrial failure, neuronal loss |
| Spinocerebellar Ataxia 35 (SCA35) | Autosomal dominant | Cerebellar degeneration |
| Myopathy | Autosomal dominant | Muscle weakness |
Chchd10 Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
The study of Chchd10 Gene has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.