gene

FRDA1

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about FRDA1: 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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Summary

FRDA1 gene encoding frataxin - a mitochondrial protein essential for iron-sulfur cluster biogenesis, linked to Friedreich ataxia and neurodegeneration

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🧬 Gene Info
Gene SymbolFRDA1
Full NameFXN (Frataxin)
AliasesFRDA1 gene encoding frataxin
Chromosome9q21.11
Amino Acids210 aa
UniProt ID[Q16595](https://www.uniprot.org/uniprotkb/Q16595/entry)
GeneCardsFRDA1
Human Protein AtlasFRDA1
Iron import regulationControls mitochondrial iron uptake through MIYAML
Iron storage coordinationWorks with mitochondrial ferritin (FTMT)
Prevents iron overloadAvoids toxic Fenton chemistry
Protects against ferroptosisMitochondrial iron-mediated cell death
HeartHighest expression - explains cardiac involvement
LiverHigh metabolic demand
KidneyEnergy-intensive transport
Associated Diseasesneurodegeneration
DatabasesGeneCardsNCBI GeneHPASTRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

FRDA1 Gene - Frataxin (FXN)

gene · 1608 words

Pathway Diagram

graph TD
    FRDA1["FRDA1"]
    neurodegeneration["neurodegeneration"]
    FRDA1 -->|"implicated_in"| neurodegeneration
    style FRDA1 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

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Mentioning Analyses (0)

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Experiments (0)

Experimental studies targeting or related to this entity

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Related Papers (0)

Scientific publications cited in analyses involving this entity

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Debates (0)

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Related Research

Hypotheses and analyses mentioning FRDA1 in their description or question text

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