| Gene Symbol | TIMM17A |
| Full Name | Translocase of Inner Mitochondrial Membrane 17A |
| Chromosome | 1q32.1 |
| Function | is an essential component of the TIM22 translocase complex located in the mitochondrial inner membrane. |
| Primary Expression | neuronal tissues |
| Molecular Weight | 17 kDa |
| Amino Acids | 171 aa |
| Exons | 6 |
| UniProt ID | O60830 (TIM17_HUMAN) |
| NCBI Gene ID | 10628 |
| Ensembl ID | ENSG00000139360 |
| GeneCards | TIMM17A |
| Human Protein Atlas | TIMM17A |
| Associated Diseases | neurodegeneration |
| Interactions | BECN1, BNIP3, BNIP3L, CEBPB, DDIT3, DNM1L |
| KG Connections | 43 knowledge graph edges |
| Databases | GeneCardsHPASTRING |
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