Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about NDUFAF8: 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.
NDUFAF8 is a mitochondrial complex I assembly factor essential for NADH dehydrogenase biogenesis and implicated in Leigh syndrome and Parkinson's disease
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| Gene Symbol | NDUFAF8 |
| Full Name | NADH Dehydrogenase Complex Assembly Factor 8 |
| Chromosome | 19q13.42 |
| Function | encodes a mitochondrial complex I assembly factor that plays a critical role in the biogenesis of the NADH dehydrogenase (complex I) of the mitochondrial respiratory chain. |
| Molecular Weight | 24 kDa |
| Amino Acids | 213 aa |
| Exons | 5 |
| UniProt ID | Q6ZMC2 |
| NCBI Gene ID | 285154 |
| Ensembl ID | ENSG00000156437 |
| OMIM | 618198 |
| GeneCards | NDUFAF8 |
| Human Protein Atlas | NDUFAF8 |
| Associated Diseases | Parkinson's disease |
| Databases | GeneCardsHPASTRING |
Knowledge base pages for this entity
graph TD
NDUFAF8["NDUFAF8"]
neurodegeneration["neurodegeneration"]
NDUFAF8 -->|"implicated_in"| neurodegeneration
style NDUFAF8 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 NDUFAF8 in their description or question text
No additional research found