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XB-GENEPAGE-5885004
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 acad9

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acyl-CoA dehydrogenase family member 9

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( Nomenclature history )

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electron transport

AI Protein Function :
acad9 encodes a mitochondrial acyl‑CoA dehydrogenase involved in fatty‑acid β‑oxidation and assembly of mitochondrial complex I; the protein localizes to mitochondria; expression is detected in the hea...[+]



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Diseases: 


Disease Ontology:
nuclear type mitochondrial complex I deficiency 20

MIM:
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20; MC1DN20

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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