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carnitine palmitoyltransferase 2

The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq]

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Data Correlations | 1,590 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

  • Drug target sets for approved compounds

    score: 100100 | Homo sapiens Homo sapiens | Therapeutic   Therapeutic

    The DrugBank database is a unique bioinformatics and cheminformatics resource that combines detailed drug (i.e. chemical, pharmacological and pharmaceutical) data with comprehensive drug target (i.e. sequence, structure, and pathway) information.

    Authors: David S Wishart, Craig Knox, An Chi Guo et al.

    Organization: Department of Computing Science, Univers…

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Thought leaders and organizations working on research involving CPT2.

  • Georgirene D Vladutiu
  • Marcus Deschauer
  • Jean-Paul Bonnefont
  • Laure Thuillier
  • Michael J Bennett
  • Rigshospitalet, Denmark
  • Assistance Publique - Hôpitaux de Paris
  • State University of New York at Buffalo
  • National University Hospital
  • University of Tokushima
  • Groupe Hospitalier Necker-Enfants Malades
  • Hadassah - Hebrew University Medical Center

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