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MECR

Official Full Name
mitochondrial trans-2-enoyl-CoA reductase
Organism
Homo sapiens
GeneID
51102
Background
The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]
Synonyms
ETR1; NRBF1; OPA16; CGI-63; FASN2B; DYTOABG;

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