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IYD, iodotyrosine deiodinase

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IYD, iodotyrosine deiodinase

  • This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

  • Gene Synonyms (C6orf71, DEHAL1, IYD-1, TDH4, iodotyrosine deiodinase 1, iodotyrosine dehalogenase 1,)
  • NCBI Gene ID: 389434
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q6PHW0
    UNIPROT ID#>>Q2VPV9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

iodotyrosine deiodinase interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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