Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about DYNLT1: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.
DYNLT1 gene encodes Tctex-1 dynein light chain, essential for retrograde axonal transport. Critical for neuronal survival and implicated in Alzheimer's, Parkinson's, and Huntington's diseases.
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| Gene Symbol | DYNLT1 |
| Full Name | Dynein Light Chain Tctex-Type 1 |
| Chromosome | 6q21 |
| Function | is a large multi-subunit motor protein complex essential for retrograde transport in all eukaryotic cells. |
| Molecular Weight | 500 kDa |
| Amino Acids | 110 aa |
| UniProt ID | P63172 |
| NCBI Gene ID | 6993 |
| Ensembl ID | ENSG00000126653 |
| OMIM | 162376 |
| GeneCards | DYNLT1 |
| Human Protein Atlas | DYNLT1 |
| DYNLT1 (Tctex-1) | The Tctex-type light chain |
| DYNLT2 | Another Tctex family member |
| DYNLRB1/DYNLRB2 (Roadblock) | The roadblock-type light chains |
| Associated Diseases | Alzheimer's disease, Parkinson's disease, Huntington's disease |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
DYNLT1["DYNLT1"]
neurodegeneration["neurodegeneration"]
DYNLT1 -->|"implicated_in"| neurodegeneration
style DYNLT1 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0| Target | Relation | Type | Str |
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Hypotheses where this entity is a therapeutic target
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Scientific analyses that reference this entity
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Experimental studies targeting or related to this entity
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Scientific publications cited in analyses involving this entity
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Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning DYNLT1 in their description or question text
No additional research found