Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about PLXNA2: 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 | PLXNA2 |
| Chromosome | 1q23.3 |
| Protein Type | Gene |
| Function | encodes a member of the plexin family of transmembrane receptors for semaphorins, playing critical roles in neural development, circuit formation, and synaptic plasticity. |
| Molecular Weight | 220 kDa |
| Amino Acids | 034 aa |
| Exons | 33 |
| GeneCards | PLXNA2 |
| Human Protein Atlas | PLXNA2 |
| Cerebellum | Purkinje cells and granule cells |
| Olfactory bulb | mitral and tufted cells |
| Thalamus | relay neurons |
| Substantia nigra | dopaminergic neurons |
| Axonal repulsion | SEMA3A binding to PLXNA2 triggers growth cone collapse through RhoA/ROCK-dependent cytoskeletal remodeling[@plexin2021] |
| Synaptic scaling | PLXNA2 modulates AMPA receptor trafficking via Rap GAP activity[@plexin2022] |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
PLXNA2["PLXNA2"]
neurodegeneration["neurodegeneration"]
PLXNA2 -->|"implicated_in"| neurodegeneration
style PLXNA2 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 PLXNA2 in their description or question text
No additional research found