Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about PEX2: 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.
PEX2 (Peroxisome Biogenesis Factor 2) gene encodes a peroxin essential for peroxisome biogenesis and peroxisomal matrix protein import. Mutations cause peroxisome biogenesis disorders including Zellweger syndrome.
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| Gene Symbol | PEX2 |
| Aliases | Peroxisome Biogenesis Factor 2, Page for PEX2 Protein |
| Chromosome | 8q21.13 |
| Protein Type | Gene |
| Function | It recognizes signal sequences in PMPs and facilitates their proper insertion. |
| Molecular Weight | 33 kDa |
| Amino Acids | 299 aa |
| Exons | 4 |
| GeneCards | PEX2 |
| Human Protein Atlas | PEX2 |
| Ubiquitination | PEX2 is ubiquitinated on its cytosolic domains, targeting it for recycling or degradation |
| Phosphorylation | Serine/threonine phosphorylation may regulate PEX2 function and interactions |
| N-myristoylation | Some evidence suggests potential myristoylation at the N-terminus |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
PEX2["PEX2"]
neurodegeneration["neurodegeneration"]
PEX2 -->|"implicated_in"| neurodegeneration
style PEX2 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 PEX2 in their description or question text
No additional research found