Title : Regulation of histone H3K4 methylation in brain development and disease.

Pub. Date : 2014 Sep 26

PMID : 25135975






1 Functional Relationships(s)
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1 The growing list of mutations implicated in monogenic disorders of the developing brain includes at least seven genes (ARX, CUL4B, KDM5A, KDM5C, KMT2A, KMT2C, KMT2D) with loss-of-function mutations affecting proper regulation of histone H3 lysine 4 methylation, a chromatin mark which on a genome-wide scale is broadly associated with active gene expression, with its mono-, di- and trimethylated forms differentially enriched at promoter and enhancer and other regulatory sequences. Lysine lysine methyltransferase 2D Homo sapiens