Mtch2 — Mitochondrial Carrier Homolog 2 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
| Mitochondrial Carrier Homolog 2 | |
|---|---|
| Gene Symbol | MTCH2 |
| Full Name | mitochondrial carrier 2 |
| Chromosome | 11p15.4 |
| NCBI Gene ID | 123591 |
| OMIM | 614215 |
| Ensembl ID | ENSG00000135249 |
| UniProt ID | Q9Y6C9 |
| Associated Diseases | Metabolic Disorders, Neurodegeneration, Cancer |
This page provides comprehensive information about the subject's role in neurodegenerative diseases. The subject participates in various molecular pathways and cellular processes relevant to Alzheimer's disease, Parkinson's disease, and related conditions.
MTCH2 (Mitochondrial Carrier Homolog 2) is a member of the mitochondrial carrier family involved in transporting metabolites across the mitochondrial inner membrane. It plays important roles in:
MTCH2 is ubiquitously expressed with high levels in:
The study of Mtch2 — Mitochondrial Carrier Homolog 2 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.