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ACAD9, acyl-CoA dehydrogenase family member 9

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ACAD9, acyl-CoA dehydrogenase family member 9

  • 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]

  • Gene Synonyms (complex I assembly factor ACAD9, mitochondrial, acyl-Coenzyme A dehydrogenase family, member 9, very-long-chain acyl-CoA dehydrogenase VLCAD, MC1DN20, NPD002,)
  • NCBI Gene ID: 28976
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9H845
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

acyl-CoA dehydrogenase family member 9 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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