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EHMT1 gene

Known as: KIAA1876, KMT1D, EUCHROMATIC HISTONE METHYLTRANSFERASE 1 
This gene is involved in histone methylation.
National Institutes of Health

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EHMT1 protein, humanGene ExpressionMethylationProtein methylation

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EHMT1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Converging molecular networks affected in Kleefstra syndrome and related neurodevelopmental disorders
Our work on the ​EHMT1​ gene and Kleefstra syndrome started from 2002 onwards, when we identified through a chromosomal… 
2017
2017
The epigenetic role of the Kleefstra syndrome protein EHMT1 in synaptic scaling and in cognition
The contribution of epigenetic factors in controlling the expression of genetic programs related to cognition and development… 
2017
2017
Biochemical Function and Association with Brain Disorders
The gene EHMT1 that encodes the Euchromatic Histone Methyltransferase-1, also known as GLP (G9a-like protein), has been… 
2016
2016
Differential patterns of histone methylase EHMT2 and its catalyzed histone modifications H3K9me1 and H3K9me2 during maturation of central auditory system
Histone methylation is an important epigenetic mark leading to changes in DNA accessibility and transcription. Here, we… 
2015
2015
Table 2. [Selected Pathogenic EHMT1 Allelic Variants].
2015
2015
Regulates Retention of G 9 a on Chromatin 1 A Role for Widely Interspaced Zinc Finger ( WIZ ) in Retention of the G 9 a Methyltransferase on Chromatin *
G9a and GLP lysine methyltransferases form a heterodimeric complex that is responsible for the majority of histone H3 lysine 9… 
2013
2013
Epigenetic Synergies Between Biotin and Folate in the Regulation of Pro‐Inflammatory Cytokines and Repeats
The protein biotin ligase, holocarboxylase synthetase (HLCS), is a chromatin protein that interacts physically with the DNA… 
2013
2013
Kleefstra Syndrome, an example of a single gene defect (EHMT1) with important neurocognitive consequences
Objective: Emerging evidence shows that different cognitive disorders, such as Intellectual disability, autism, and schizophrenia… 
2010
2010
Corrigendum to: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
Correction to: European Journal of Human Genetics advance online publication 7 October 2009; doi: 10.1038/ejhg.2009.152 Since the… 
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