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DNMT3B is a DNA methyltransferase enzyme responsible for establishing new DNA methylation patterns during embryonic development. It plays a critical role in normal mammalian development, genomic imprinting, X-chromosome inactivation, and regulation of gene expression. Mutations in DNMT3B are associated with immunodeficiency-centromeric instability-facial anomalies syndrome (ICF) and have been implicated in cancer and other developmental disorders.
Catalyzes the transfer of a methyl group to the 5-position of cytosine residues in DNA at CpG dinucleotides, leading to transcriptional repression.
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