Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about CPLX4: 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.
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| Gene Symbol | CPLX4 |
| Aliases | Complexin-4 |
| Chromosome | 11q13.2 |
| Function | CPLX4 encodes complexin 4, a neuronal protein involved in regulating synaptic vesicle fusion. |
| Primary Expression | various brain regions, with particularly high expression in retina and sensory neurons |
| Molecular Weight | 34 kDa |
| Amino Acids | 312 aa |
| Exons | 5 |
| UniProt ID | Q8WXD5 |
| NCBI Gene ID | 285315 |
| Ensembl ID | ENSG00000177054 |
| GeneCards | CPLX4 |
| Human Protein Atlas | CPLX4 |
| Associated Diseases | Autism spectrum disorder, synaptic transmission disorders, neurodegenerative diseases |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
CPLX4["CPLX4"]
neurodegeneration["neurodegeneration"]
CPLX4 -->|"implicated_in"| neurodegeneration
style CPLX4 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
No analyses mention this entity
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. Cost |
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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 CPLX4 in their description or question text
No additional research found