Details
| Type | Mitochondrial Transfer RNA |
| Official Symbol | MT-TM |
| Official Name | mitochondrially encoded tRNA-Met (AUA/G) [Source:HGNC Symbol;Acc:HGNC:7492] |
| Ensembl ID | ENSG00000210112 |
| Bio databases IDs | |
| Aliases | mitochondrially encoded tRNA-Met (AUA/G) |
| Synonyms | Met-tRNA, Mitochondrial t-M, mt-Tm-201, tRNA-Met, TRNM |
| Species | Human, Homo sapiens |
Protein Domains
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human MT-TM often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- triplet codon-amino acid adaptor
Pathways
Biological processes and signaling networks where the MT-TM 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.
disease
- mitochondrial disorder
- MELAS syndrome
- mitochondrial myopathy
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Cytoplasm
- Mitochondria