gene

NDUFS8

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about NDUFS8: 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.

41Connections
0Hypotheses
0Analyses
23Outgoing
18Incoming
0Experiments
0Debates

Summary

Comprehensive gene page for NDUFS8, encoding a critical iron-sulfur subunit of mitochondrial Complex I, implicated in Parkinson's disease, Leigh syndrome, and other neurodegenerative disorders

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🧬 Gene Info
Gene SymbolNDUFS8
Full NameNADH:Ubiquinone Oxidoreductase Core Subunit S8
Chromosome19q13.42
Functionencodes a critical iron-sulfur protein subunit of mitochondrial Complex I (NADH:ubiquinone oxidoreductase), the largest and most complex enzyme of the mitochondrial electron transport chain.
Primary ExpressionBrain, Heart, Skeletal Muscle, Liver, Kidney
Molecular Weight23 kDa
Amino Acids210 aa
Exons5
UniProt IDP51970
NCBI Gene ID4728
Ensembl IDENSG00000110717
OMIM602140
GeneCardsNDUFS8
Human Protein AtlasNDUFS8
Associated DiseasesParkinson's Disease, Leigh Syndrome, Mitochondrial Complex I Deficiency
KG Connections41 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: NDUFS8 — AlphaFold P51970 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

NDUFS8 — NADH:Ubiquinone Oxidoreductase Core Subunit S8

gene · 2606 words

Pathway Diagram

graph TD
    NDUFS8["NDUFS8"]
    Alzheimer{"Alzheimer"}
    NDUFS8 -->|"expressed in"| Alzheimer
    Cancer{"Cancer"}
    NDUFS8 -->|"expressed in"| Cancer
    ALZHEIMER_S_DISEASE["ALZHEIMER'S DISEASE"]
    NDUFS8 -->|"expressed in"| ALZHEIMER_S_DISEASE
    CYTOKINES["CYTOKINES"]
    NDUFS8 -->|"expressed in"| CYTOKINES
    LDLR["LDLR"]
    NDUFS8 -->|"expressed in"| LDLR
    ALZHEIMER_DISEASE["ALZHEIMER DISEASE"]
    NDUFS8 -->|"expressed in"| ALZHEIMER_DISEASE
    MITOCHONDRIAL_DYSFUNCTION["MITOCHONDRIAL DYSFUNCTION"]
    NDUFS8 -->|"expressed in"| MITOCHONDRIAL_DYSFUNCTION
    CLU["CLU"]
    NDUFS8 -->|"regulates"| CLU
    SPG7["SPG7"]
    NDUFS8 -->|"regulates"| SPG7
    MAPT["MAPT"]
    NDUFS8 -->|"regulates"| MAPT
    Epigenetic(["Epigenetic"])
    NDUFS8 -->|"expressed in"| Epigenetic
    Dna_Methylation(["Dna Methylation"])
    NDUFS8 -->|"expressed in"| Dna_Methylation
    ACE["ACE"]
    ACE -->|"expressed in"| NDUFS8
    PHGDH["PHGDH"]
    PHGDH -->|"biomarker for"| NDUFS8
    HK2["HK2"]
    HK2 -->|"biomarker for"| NDUFS8
    CANCER["CANCER"]
    CANCER -->|"expressed in"| NDUFS8
    SMAD3["SMAD3"]
    SMAD3 -->|"biomarker for"| NDUFS8
    style NDUFS8 fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (23)

TargetRelationTypeStr
benchmark_ot_ad_answer_key:NDUFS8data_indataset_row0.00
ds-83b31ef18d49provides_data_fordataset1.00
Alzheimer Diseaserisk_factor_fordisease0.85
Alzheimerexpressed_indisease0.65
Cancerexpressed_indisease0.65

Incoming (18)

SourceRelationTypeStr
benchmark_ot_ad_answer_key:NDUFS8data_indataset_row0.00
ds-83b31ef18d49data_indataset1.00
GENESregulatesgene0.60
MITOCHONDRIAL DYSFUNCTIONexpressed_ingene0.60
ALZHEIMER DISEASEexpressed_ingene0.60

Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
No targeting hypotheses

Mentioning Analyses (0)

Scientific analyses that reference this entity

No analyses mention this entity

Experiments (0)

Experimental studies targeting or related to this entity

ExperimentTypeDiseaseScoreFeasibilityModelStatusEst. Cost
No experiments found

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found

Debates (0)

Multi-agent debates referencing this entity

No debates reference this entity

Related Research

Hypotheses and analyses mentioning NDUFS8 in their description or question text

No additional research found