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ARUP Laboratories
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  • Mutation Databases
    • ALPORT (COL4A5)
      • ALPORT Database
      • ALPORT Links
      • ALPORT Submissions
    • Biotinidase Deficiency (BTD)
      • BTD Database
      • BTD Links
      • BTD Submissions
    • Galactosemia (GALT)
      • GALT Database
      • GALT Links
      • GALT Submissions
    • HHT (ACVRL1 and ENG)
      • ACVRL1 Database
      • ENG Database
    • Juvenile Polyposis Syndrome (SMAD4)
      • SMAD4 Database
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    • Legius Syndrome (SPRED1)
      • SPRED1 Database
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    • MEN1 (Menin)
      • MEN1 Database
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      • MEN1 Submissions
    • MEN2 (RET)
      • MEN2 Database
      • MEN2 Links
      • MEN2 Submissions
    • Primary Carnitine Deficiency (SLC22A5)
      • SLC22A5 Database
      • SLC22A5 Links
      • SLC22A5 Submissions
    • Pulmonary Arterial Hypertension (BMPR2)
      • BMPR2 Database
      • BMPR2 Links
      • BMPR2 Submissions
    • RASA1-Related Disorders
      • RASA1 Database
      • RASA1 Links
      • RASA1 Submissions

MEN2 References

The web links shown below are existing online resources for MEN2 and the RET proto-oncogene. Links to several review journal articles are given, as well as genome and protein links.

Please contact us to suggest additional content for this page.

Databases

  • Cosmic Database: RET somatic mutations in cancer
  • The Human Gene Mutation Database (HGMD®)or Uniprot: For Hirschsprung RET mutations

Web Reviews

  • Entrez Gene: RET proto-oncogene
  • GeneReviews for MEN2 on the GeneTest website
  • OMIM for RET, MEN2A (and FMTC), MEN2B, and Hirschsprung disease

Peer-Reviewed Literature

  • Kloos, et al. Medullary thyroid cancer: management guidelines of the American Thyroid Association. Thyroid 2009. 19(6):565-612.
  • Kouvaraki, et al. RET proto-oncogene: A review and update of Genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors. Thyroid 2005. 15(6): 531-544.
  • de Groot, et al. RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors. Endocrine Reviews 2006. 27(5): 535-60.
  • Eng, et al. The relationship between specific RET mutations and disease phenotype in multiple endocrine neoplasia. JAMA 1996. 276(19): 1575-1579.
  • Brandi, et al. Consensus: Guidelines for Diagnosis and Therapy of MEN Type 1 and Type 2. Journal of Clinical Endocrinology & Metabolism 2001. 86 (12): 5658-5671.
    • MEN2 Home
    • MEN2 Database
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    • MEN2 Submissions
  • About ARUP Laboratories

    ARUP Laboratories is a national reference laboratory that supports the testing needs of hospitals and laboratories throughout the U.S. ARUP also serves as a training site for pathology residency and fellowship programs.

    Visiting ARUP Laboratories
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  • Contact Information
    • MEN2 Mutations
      Rong Mao, MD
      Medical Director
      Molecular Genetics
      (801) 583-2787, x3165
      rong.mao@aruplab.com
    • MEN2 Submissions
      Rebecca Margraf, PhD
      R&D Investigator
      Advanced Technology Group
      (801) 583-2787 x2218
      rebecca.margraf@aruplab.com
    • MEN2 Testing
      ARUP Client Services
      ARUP Laboratories
      (800) 522-2787
      clientservices@aruplab.com
    • Website
      David Crockett, PhD
      Director, Bioinformatics
      (801) 583-2787, x2388
      david.crockett@utah.edu
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