XB-GENEPAGE-988136
???displayGene.symbol???:
myt1l
???displayGene.name???:
myelin transcription factor 1 like
???displayGene.synonyms???
LOC108717166
,
LOC108718228
(
Nomenclature history )
???displayGene.geneFunction???
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...[+]
???displayGene.geneInteractants???
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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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