| Gene Symbol | TIMM22 |
| Chromosome | 17p13.2 |
| Protein Family | Translocase of inner mitochondrial membrane (TIM) family |
| Function | is an essential component of the TIM22 complex, which mediates the insertion of carrier proteins into the mitochondrial inner membrane. |
| Primary Expression | Mitochondrial inner membrane |
| Subcellular Localization | Mitochondrial inner membrane |
| Molecular Weight | 25 kDa |
| Amino Acids | 227 aa |
| UniProt ID | Q9Y5J7 |
| GeneCards | TIMM22 |
| Human Protein Atlas | TIMM22 |
| Associated Diseases | Parkinson's Disease, Mitochondrial Disorders |
| Interactions | BECN1, BNIP3, BNIP3L, CEBPB, DDIT3, DNM1L |
| KG Connections | 43 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |
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