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TMEM126A

Official Full Name
transmembrane protein 126A
Organism
Homo sapiens
GeneID
84233
Background
The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
Synonyms
OPA7;

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