Gene

ACADS

Species
Homo sapiens
Symbol
ACADS
Name
acyl-CoA dehydrogenase short chain
Synonyms
  • ACAD3
  • acyl-CoA dehydrogenase, C-2 to C-3 short chain
Biotype
protein coding gene
Automated Description
Enables acyl-CoA dehydrogenase activity. Involved in fatty acid beta-oxidation using acyl-CoA dehydrogenase. Located in centrosome; mitochondrion; and nucleoplasm. Implicated in alcohol use disorder and short chain acyl-CoA dehydrogenase deficiency.
RGD Description
This gene encodes a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with short-chain acyl-CoA dehydrogenase (SCAD) deficiency. Alternative splicing results in two variants which encode different isoforms. [provided by RefSeq, Oct 2014]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR43884
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
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      Transgenic construct
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          ACADS molecule type
          Interactor gene
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            Genetic Interactions

            ACADS role
            ACADS genetic perturbation
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            Interactor role
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