ACAD9 Gene Summary [Human]

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]

Details

Type
Processed Transcript
Official Symbol
ACAD9
Official Name
acyl-CoA dehydrogenase family member 9 [Source:HGNC Symbol;Acc:HGNC:21497]
Ensembl ID
ENSG00000177646
Bio databases IDs NCBI: 28976 Ensembl: ENSG00000177646
Aliases acyl-CoA dehydrogenase family member 9
Synonyms 2600017P15RIK, 4732402K02, acyl-CoA dehydrogenase family member 9, acyl-CoA dehydrogenase family, member 9, acyl-Coenzyme A dehydrogenase family, member 9, C630012L17RIK, MC1DN20, NPD002, NYGGF2
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human ACAD9 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Acyl-CoA dehydrogenase, C-terminal domain
  • acyl-CoA dehydrogenase
  • Acyl-CoA dehydrogenase, middle domain
  • enzyme
  • protein binding
  • long-chain-acyl-CoA dehydrogenase
  • Acyl-CoA dehydrogenase, N-terminal domain

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • ACAD9 deficiency
  • Mitochondrial complex I deficiency
  • insulin resistance
regulated by
regulates
  • Mitochondrial ETC 1
  • long chain fatty acid

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • Nucleus
  • Mitochondria
  • mitochondrial membrane
  • mitochondrial inner membrane
  • dendrites

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human ACAD9 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • long-chain fatty acid metabolic process
  • medium-chain fatty acid metabolic process
  • mitochondrial respiratory chain complex I assembly

Cellular Component

Where in the cell the gene product is active
  • nucleus
  • dendrite
  • mitochondrial membrane
  • mitochondrion
  • mitochondrial inner membrane

Molecular Function

What the gene product does at the molecular level
  • acyl-CoA dehydrogenase activity
  • protein binding
  • medium-chain-acyl-CoA dehydrogenase activity
  • flavin adenine dinucleotide binding
  • long-chain-acyl-CoA dehydrogenase activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.