Details
| Type | Protein Coding |
| Official Symbol | TIMM22 |
| Official Name | translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317] |
| Ensembl ID | ENSG00000277649 |
| Bio databases IDs | |
| Aliases | translocase of inner mitochondrial membrane 22 |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43