Details
| Type | Mitochondrial Transfer RNA |
| Official Symbol | MT-TS2 |
| Official Name | mitochondrially encoded tRNA-Ser (AGU/C) 2 [Source:HGNC Symbol;Acc:HGNC:7498] |
| Ensembl ID | ENSG00000210184 |
| Bio databases IDs | |
| Aliases | mitochondrially encoded tRNA-Ser (AGU/C) 2 |
| Synonyms | mt-Ts1, mt-Ts1-201, tRNA-Ser, TrnS1, TRNS2 |
| 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-TS2 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
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- diabetes mellitus
- retinitis pigmentosa-deafness syndrome
- cataract disease
- MELAS syndrome
- cerebellar ataxia, cataract and diabetes mellitus
- mitochondrial disorder
- cerebellar ataxia
- MERRF/MELAS overlap syndrome
regulated by
- POR
- N-[2,2,2-trichloro-1-(2-naphthylamino)ethyl]-2-furamide
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