Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about COQ2: 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.
COQ2 encodes the para-hydroxybenzoate polyprenyltransferase, the rate-limiting enzyme in coenzyme Q (CoQ10) biosynthesis, with variants causing mitochondrial disorders and potential relevance to Parkinson's disease.
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| Gene Symbol | COQ2 |
| Full Name | Coenzyme Q Biosynthesis Protein COQ2 |
| Aliases | CoQ10 |
| Chromosome | 4q22.1 |
| Protein Type | Enzyme |
| Function | is a mitochondrial enzyme that catalyzes the rate-limiting step in coenzyme Q (CoQ10, ubiquinone) biosynthesis. |
| Molecular Weight | 20 kDa |
| Amino Acids | 421 aa |
| GeneCards | COQ2 |
| Human Protein Atlas | COQ2 |
| COQ4 | Complex scaffold |
| COQ6 | Hydroxylase |
| COQ7 | Hydroxylase (COQ7 is also called COQ5 in some organisms) |
| COQ8A/COQ8B | Kinases |
| COQ9 | Lipid-binding chaperone |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
COQ2["COQ2"]
neurodegeneration["neurodegeneration"]
COQ2 -->|"implicated_in"| neurodegeneration
style COQ2 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 COQ2 in their description or question text
No additional research found