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SLC25A22

Official Full Name
solute carrier family 25 member 22
Organism
Homo sapiens
GeneID
79751
Background
This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jul 2010]
Synonyms
GC1; DEE3; GC-1; EIEE3; NET44;

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