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vacuolar protein sorting 13 homolog A (S. cerevisiae)

The protein encoded by this gene may control steps in the cycling of proteins through the trans-Golgi network to endosomes, lysosomes and the plasma membrane. Mutations in this gene cause the autosomal recessive disorder, chorea-acanthocytosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq]

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Data Correlations | 1,265 studies

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Individual Studies
  • Mouse Phenotypes - Autosomal recessive hereditary disorder

    score: 100100 | Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data

  • OMIM - Movement 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

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Thought leaders and organizations working on research involving VPS13A.

  • Adrian Danek
  • Mio Ichiba
  • Carol Dobson-Stone
  • Akira Sano
  • Masayuki Nakamura
  • Kagoshima University Graduate School of Medical and Dental Sciences
  • University of Oxford
  • University of Georgia
  • Medical University of Vienna
  • Instituto Nacional de Enfermedades Respiratorias

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