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FDX1L

Official Full Name
ferredoxin 2
Organism
Homo sapiens
GeneID
112812
Background
This gene encodes a member of the ferredoxin family. The encoded protein contains a 2Fe-2S ferredoxin-type domain and is essential for heme A and Fe/S protein biosynthesis. Mutation in FDX1L gene is associated with mitochondrial muscle myopathy. [provided by RefSeq, Sep 2014]
Synonyms
FDX2; FDX1L; MEOAL;

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