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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MITF-20-RE | 20 (40 μL) | 200 μL |  |
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| MITF-20-OR | 20 (40 μL) | 200 μL |  |
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| MITF-20-GO | 20 (40 μL) | 200 μL |  |
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| MITF-20-GR | 20 (40 μL) | 200 μL |  |
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| MITF-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : MITF
Gene Name : Melanogenesis associated transcription factor
Chromosome : CHR 3: 697,394,34-699,683,36
Locus : 3p13
Alt. Genes : FAM13A
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