gene

MTCO1

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about MTCO1: 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 Info
Gene SymbolMT
Full NameCO1 Gene - Mitochondrially Encoded Cytochrome C Oxidase I
AliasesMTCO1
FunctionCytochrome b is a key component of Complex III (ubiquinol-cytochrome c reductase), which catalyzes the transfer of electrons from ubiquinol to cytochrome c.
GeneCardsMT
Human Protein AtlasMT
Catalytic centerContains heme a and heme a3, where O2 binding and reduction occur
Electron transferReceives electrons from cytochrome c and transfers to O2
Proton pumpingContributes to proton pumping across the inner membrane
EvolutionEncoded by mtDNA in all animals (co-evolution with nuclear-encoded subunits)
HemenessHeme a and heme a3 are unique prosthetic groups
Pediatric disordersMT-CO1 mutations cause severe infantile mitochondrial disorders
EncephalomyopathyGlobal developmental delay, lactic acidosis, cardiomyopathy
HeteroplasmyDisease manifestation depends on mutant mtDNA load
m.7445A>GCan cause combined LHON and sideroblastic anemia
DatabasesGeneCardsUniProtNCBI GeneHPASTRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

MT-CO1 Gene - Mitochondrially Encoded Cytochrome C Oxidase I

gene · 548 words

Pathway Diagram

graph TD
    MTCO1["MTCO1"]
    neurodegeneration["neurodegeneration"]
    MTCO1 -->|"implicated_in"| neurodegeneration
    style MTCO1 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Targeting Hypotheses (0)

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Mentioning Analyses (0)

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Experiments (0)

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Related Papers (0)

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Related Research

Hypotheses and analyses mentioning MTCO1 in their description or question text

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