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MBD5 gene

Known as: FLJ11113, methyl-CpG binding domain protein 5, KIAA1461 
National Institutes of Health

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Related topics

1 relation
MBD4 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome
2q23.1 microdeletion syndrome is characterized by intellectual disability, motor delay, autistic‐like behaviors, and a… 
2014
2014
MBD5 regulates iron metabolism via methylation‐independent genomic targeting of Fth1 through KAT2A in mice
Ferritin plays important roles in iron metabolism and controls iron absorption in the intestine. The ferritin subunits ferritin… 
2014
2014
Intragenic MBD5 familial deletion variant does not negatively impact MBD5 mRNA expression
Abstract2q23.1 deletion syndrome is characterized by intellectual disability, speech impairment, seizures, disturbed sleep… 
Highly Cited
2013
Highly Cited
2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder
Copy number variations associated with abnormal gene dosage have an important role in the genetic etiology of many… 
2012
2012
The Essential Role of Mbd5 in the Regulation of Somatic Growth and Glucose Homeostasis in Mice
Methyl-CpG binding domain protein 5 (MBD5) belongs to the MBD family proteins, which play central roles in transcriptional… 
Highly Cited
2010
Highly Cited
2010
The Human Proteins MBD5 and MBD6 Associate with Heterochromatin but They Do Not Bind Methylated DNA
Background MBD5 and MBD6 are two uncharacterized mammalian proteins that contain a putative Methyl-Binding Domain (MBD). In the… 
Highly Cited
2010
Highly Cited
2010
Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures
Microdeletion of chromosome 2q23.1 results in a novel syndrome previously reported in five individuals. Many of the del(2)(q23.1… 
Highly Cited
2010
Highly Cited
2010
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
Six submicroscopic deletions comprising chromosome band 2q23.1 in patients with severe mental retardation (MR), short stature… 
2010
2010
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype
Correction to: European Journal of Human Genetics (2010) 18, 163–170; doi:10.1038/ejhg.2009.152; published online 7 October 2009… 
Highly Cited
2003
Highly Cited
2003
Comparative study of methyl-CpG-binding domain proteins
BackgroundMethylation at CpG dinucleotides in genomic DNA is a fundamental epigenetic mechanism of gene expression control in… 
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