Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about NDUFA13: 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 | NDUFA13 |
| Protein Type | Gene |
| Function | ### Structural Role in Complex I |
| GeneCards | NDUFA13 |
| Human Protein Atlas | NDUFA13 |
| Leigh Syndrome | A severe neurodegenerative disorder presenting with developmental regression, hypotonia, ataxia, and characteristic lesions in the brainstem and basal ganglia [@leigh_syndrome] |
| Cardiomyopathy | Hypertrophic or dilated cardiomyopathy due to cardiac muscle energy failure |
| Encephalomyopathy | Combined neurological and muscular involvement |
| Growth Retardation | Failure to thrive due to impaired energy metabolism |
| Associated Diseases | neurodegeneration |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
NDUFA13["NDUFA13"]
neurodegeneration["neurodegeneration"]
NDUFA13 -->|"implicated_in"| neurodegeneration
style NDUFA13 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
| Hypothesis | Score | Disease | Analysis |
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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
| Title & PMID | Authors | Journal | Year | Citations |
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Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning NDUFA13 in their description or question text
No additional research found