Fancc 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.
| Fanconi Anemia Group C | |
|---|---|
| Gene Symbol | FANCC |
| Full Name | Fanconi Anemia Group C |
| Chromosome | 9q22.32 |
| NCBI Gene ID | 2176 |
| OMIM | 603234 |
| Ensembl ID | ENSG00000163930 |
| UniProt ID | Q00597 |
| Associated Diseases | Fanconi Anemia, Breast Cancer |
FANCC encodes a key component of the Fanconi anemia core complex that functions in DNA interstrand crosslink repair. It interacts with several other FA proteins and is essential for maintaining genomic stability.
FANCC is a critical component of the FA core complex with multiple protein-protein interaction domains.
Key functions include:
FANCC is expressed ubiquitously:
The study of Fancc 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.
FANCC is involved in the Fanconi anemia DNA repair pathway.