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SLC25A46

Official Full Name
solute carrier family 25 member 46
Organism
Homo sapiens
GeneID
91137
Background
This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]
Synonyms
PCH1E; HMSN6B;

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