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XB-GENEPAGE-988136
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 myt1l

???displayGene.name???: 
myelin transcription factor 1 like

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LOC108717166 , LOC108718228 ( Nomenclature history )

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transcription factor containing C2HC type zinc finger

AI Protein Function :
myt1l encodes a nuclear zinc‑finger transcription factor that acts as a transcriptional repressor to promote neuronal differentiation, maintain neuronal identity, and suppress non‑neuronal gene express...[+]



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Diseases: 


Disease Ontology:
autosomal dominant intellectual developmental disorder 39

MIM:
INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39; MRD39

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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