| 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 |
| Gene | TIMM22 |
| Mol. Weight | 22 kDa |
| Associated Diseases | Parkinson's Disease, Mitochondrial Disorders |
| Interactions | HSPE1, OPA1, LAMP2, BNIP3L, SIRT1, HTRA2 |
| KG Connections | 43 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |