Details
| Type | Protein Coding |
| Official Symbol | TIMM22 |
| Official Name | translocase of inner mitochondrial membrane 22 [Source:HGNC Symbol;Acc:HGNC:17317] |
| Ensembl ID | ENSG00000278501 |
| Bio databases IDs | |
| Aliases | translocase of inner mitochondrial membrane 22 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the TIMM22 gene in human plays a role, providing insight into its function and relevance in health or disease.
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