| Gene Symbol | MFN1 |
| Aliases | MFN1PROTEIN |
| Chromosome | 3q26.33 |
| Function | Mitofusin 1 (MFN1) is a dynamin-like GTPase essential for mitochondrial outer membrane fusion |
| Primary Expression | hippocampus, Cerebellum, Cortex, Striatum, Substantia Nigra |
| Molecular Weight | 83 kDa |
| Pathways | Apoptosis, Autophagy, Epigenetic, Lysosomal Degradation, Mitochondrial Function |
| GeneCards | MFN1 |
| Human Protein Atlas | MFN1 |
| MFN2 (Mitofusin-2) | Homologous fusion protein; mutations cause Charcot-Marie-Tooth disease |
| Associated Diseases | AD, ALI, Als, Alzheimer, COPD |
| Interactions | ABCD3, Actin, AGING, AKT, ALS, ALZHEIMER |
| KG Connections | 921 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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