Scad
Scad - human acads wild type allele is located within 12q22 qter and is approximately 14 kb in length. This allele, which encodes short chain specific acyl coa dehydrogenase, mitochondrial protein, is involved in lipid oxidation. Mutations in the gene are associated with short chain acyl coa dehydrogenase deficiency.
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Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on Scad for any updates.
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