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acyl-Coenzyme A dehydrogenase, C-2 to C-3 short chain

This gene encodes a 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 Deficiency. [provided by RefSeq]

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Data Correlations | 1,108 studies

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Individual Studies
  • OMIM - Congenital disorder

    score: 100100 | Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data

  • Kidney response to hypoxia in FHH and FHH12BN consomic rats

    score: 9999 | Rattus norvegicus Rattus norvegicus | RNA Expression   RNA Expression

    Examination of gene expression changes during hypoxia of the fawn-hooded hypertensive (FHH) rat and FHH12BN consomic rat. FHH12BN rats are derived from introgression of chromosome 12 from the Brown Norway (BN) rat into the FHH genetic background.

    Source: NextBio Library/Metabolic disorders and Obesity

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Thought leaders and organizations working on research involving ACADS.

  • Niels Gregersen
  • Jerry Vockley
  • Dietrich Matern
  • Peter Bross
  • Lars Bolund
  • Department of Veterans Affairs
  • National Institute of Mental Health (NIMH)
  • Centocor, Inc.
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases …
  • National Cancer Institute (NCI)
  • Aarhus University Hospital and Faculty of Health Sciences
  • University of Aarhus
  • University of Amsterdam
  • Institute of Epidemiology
  • Aarhus University Hospital

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