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peroxisomal membrane protein 3, 35kDa

This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq]

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Data Correlations | 1,419 studies

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Individual Studies
  • HeLa cells synchronized then released from S and mitosis phases

    score: 100100 | Homo sapiens Homo sapiens | RNA Expression   RNA Expression

    HeLa S3 cells were synchronized by three different methods (double thymidine block, thymidine-nocodazole block or mitotic shake-off)in five independent time courses.

    Authors: Whitfield Michael, Demeter Janos

    Organization: Stanford Microarray Database (SMD) Stanf…

  • OMIM - Congenital disorder

    score: 9999 | 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 PXMP3.

  • Véronique Berteaux-Lecellier
  • Denise Zickler
  • J Gärtner
  • N Shimozawa
  • Y Fujiki
  • Université Paris-Sud
  • Universität Zürich
  • Heinrich Heine University Düsseldorf
  • Institute of Cell Biology
  • Seattle Biomedical Research Institute

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