NP_054768.2
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NCBI GenBank Nucleotide #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
68,760 Da
NCBI Official Full Name
acyl-CoA dehydrogenase family member 9, mitochondrial
NCBI Official Synonym Full Names
acyl-CoA dehydrogenase family, member 9
NCBI Official Synonym Symbols
NCBI Protein Information
acyl-CoA dehydrogenase family member 9, mitochondrial; very-long-chain acyl-CoA dehydrogenase VLCAD; acyl-Coenzyme A dehydrogenase family, member 9
UniProt Protein Name
Acyl-CoA dehydrogenase family member 9, mitochondrial
UniProt Synonym Gene Names
UniProt Entry Name
ACAD9_HUMAN
NCBI Summary for ACAD9
This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
UniProt Comments for ACAD9
ACAD9: Has a dehydrogenase activity on palmitoyl-CoA (C16:0) and stearoyl-CoA (C18:0). It is three times more active on palmitoyl-CoA then on stearoyl-CoA. Has little activity on octanoyl-CoA (C8:0), butyryl-CoA (C4:0) or isovaleryl-CoA (5:0). Belongs to the acyl-CoA dehydrogenase family.
Protein type: Mitochondrial; Oxidoreductase; EC 1.3.99.-
Chromosomal Location of Human Ortholog: 3q21.3
Cellular Component: mitochondrion; dendrite; nucleus
Molecular Function: acyl-CoA dehydrogenase activity; protein binding; FAD binding
Biological Process: mitochondrial respiratory chain complex I assembly
Disease: Acyl-coa Dehydrogenase Family, Member 9, Deficiency Of
Research Articles on ACAD9
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Products associated with ACAD9 elisa kit
Diseases associated with ACAD9 elisa kit
Organs/Tissues associated with ACAD9 elisa kit
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