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MITF, melanocyte inducing transcription factor

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MITF, melanocyte inducing transcription factor

  • The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]

  • Gene Synonyms (CMM8, COMMAD, MI, WS2, WS2A, bHLHe32, microphthalmia-associated transcription factor, class E basic helix-loop-helix protein 32, melanogenesis associated transcription factor, microphtalmia-associated transcription factor,)
  • NCBI Gene ID: 4286
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A087WXU1
    UNIPROT ID#>>Q8WYR3
    UNIPROT ID#>>O75030
    UNIPROT ID#>>B4DNC7
  • 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.

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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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