ACAD9

ACAD9
Identifiers
Aliases	ACAD9, NPD002, acyl-CoA dehydrogenase family member 9, MC1DN20
External IDs	OMIM: 611103; MGI: 1914272; HomoloGene: 8539; GeneCards: ACAD9; OMA:ACAD9 - orthologs
Gene location (Human)
Chr.	Chromosome 3 (human)
End	128,924,003 bp
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)
End	36,147,002 bp
RNA expression pattern
	Top expressed in
	skin of arm; ; skin of abdomen; ; myocardium of left ventricle; ; tibialis anterior muscle; ; cardiac muscle tissue of right atrium; ; skin of leg; ; mucosa of ileum; ; skin of thigh; ; right adrenal cortex; ; apex of heart;
	Top expressed in
	right kidney; ; esophagus; ; lip; ; ventricular zone; ; neural layer of retina; ; dentate gyrus of hippocampal formation granule cell; ; muscle of thigh; ; genital tubercle; ; tail of embryo; ; primary visual cortex;
	More reference expression data
	n/a
Gene ontology
Molecular function	oxidoreductase activity, acting on the CH-CH group of donors; oxidoreductase activity; protein binding; acyl-CoA dehydrogenase activity; flavin adenine dinucleotide binding; long-chain-acyl-CoA dehydrogenase activity; medium-chain-acyl-CoA dehydrogenase activity; fatty-acyl-CoA binding; very-long-chain-acyl-CoA dehydrogenase activity;
Cellular component	mitochondrial inner membrane; dendrite; mitochondrion; nucleus; mitochondrial membranes;
Biological process	mitochondrial respiratory chain complex I assembly; long-chain fatty acid metabolic process; medium-chain fatty acid metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	28976
	229211
	ENSG00000177646
	ENSMUSG00000027710
	Q9H845
	Q8JZN5
	NM_014049
	NM_172678
	NP_054768
	NP_766266
	Wikidata
View/Edit Human	View/Edit Mouse

Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene. Mitochondrial Complex I Deficiency with varying clinical manifestations has been associated with mutations in ACAD9.