NP_071957.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Related Accession #
Molecular Weight
44,765 Da
NCBI Official Full Name
short-chain specific acyl-CoA dehydrogenase, mitochondrial
NCBI Official Synonym Full Names
acyl-CoA dehydrogenase, C-2 to C-3 short chain
NCBI Official Synonym Symbols
NCBI Protein Information
short-chain specific acyl-CoA dehydrogenase, mitochondrial; butyryl-CoA dehydrogenase; short-chain acyl-CoA dehydrogenase; short chain acyl-coenzyme A dehydrogenase; acyl-Coenzyme A dehydrogenase, short chain; acetyl-Coenzyme A dehydrogenase, short chain; acyl-Coenzyme A dehydrogenase, C-2 to C-3 short chain
UniProt Protein Name
Short-chain specific acyl-CoA dehydrogenase, mitochondrial
UniProt Synonym Protein Names
Butyryl-CoA dehydrogenase
UniProt Synonym Gene Names
UniProt Entry Name
ACADS_RAT
UniProt Comments for ACADS
ACADS: Defects in ACADS are the cause of acyl-CoA dehydrogenase short-chain deficiency (ACADSD). It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults. Belongs to the acyl-CoA dehydrogenase family.
Protein type: Mitochondrial; Oxidoreductase; Lipid-binding; Amino Acid Metabolism - valine, leucine and isoleucine degradation; Carbohydrate Metabolism - butanoate; EC 1.3.8.1; Lipid Metabolism - fatty acid
Cellular Component: mitochondrion; mitochondrial matrix; mitochondrial membrane; nucleus
Molecular Function: acyl-CoA dehydrogenase activity; butyryl-CoA dehydrogenase activity; FAD binding; acyl-CoA binding
Biological Process: response to starvation; fatty acid beta-oxidation; response to glucocorticoid stimulus; fatty acid beta-oxidation using acyl-CoA dehydrogenase; protein homotetramerization; butyrate catabolic process
Research Articles on ACADS
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Pathways associated with ACADS elisa kit
Diseases associated with ACADS elisa kit
Organs/Tissues associated with ACADS elisa kit
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