| Gene Symbol | TOR1A |
| Full Name | Torsin Family 1 Member A |
| Aliases | TOR1APROTEIN |
| Chromosome | 9q34.11 |
| Function | is a glutamate deletion (ΔE302/303) that causes early-onset generalized dystonia (DYT1), one of the most common hereditary movement disorders [2](https://pubmed. |
| Subcellular Localization | </strong></td><td>Endoplasmic Reticulum, Nuclear Envelope</td></tr> |
| Molecular Weight | 38 kDa |
| Amino Acids | 332 aa |
| UniProt ID | [O95631](https://www.uniprot.org/uniprot/O95631) |
| Ensembl ID | ENSG00000136827 |
| OMIM | 605204 |
| GeneCards | TOR1A |
| Human Protein Atlas | TOR1A |
| Associated Diseases | Als |
| KG Connections | 10 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |