MYT1L encodes a member of the zinc finger superfamily of transcription factors. T Myelin transcription factor 1-like protein belongs to a novel class of cystein-cystein-histidine-cystein zinc finger proteins that function in the developing mammalian central nervous system. Forced expression of this gene in combination with the basic helix-loop-helix transcription factor NeuroD1 and the transcription factors POU class 3 homeobox 2 and achaete-scute family basic helix-loop-helix transcription factor 1 can convert fetal and postnatal human fibroblasts into induced neuronal cells, which are able to generate action potentials. Mutations in MYT1L have been associated with autosomal mental retardation-39 and autism spectrum disorder. Alternative splicing results in multiple variants.
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