about
P688
DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication fociBrahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencingInteraction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardationMeCP2, a key contributor to neurological disease, activates and represses transcriptionRett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressorATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brainDNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulationLoss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndromeStructure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
P921
Q22254582-F8C004F4-FB68-46BD-B480-20EA7653A56AQ24294291-06B5836A-D597-4F71-80F5-FE9B798FC93AQ24296972-69C2688D-D3C8-4D15-BA66-7C0D141BF2DEQ24647533-2AD9DCF9-AA6C-440D-8ED1-1BE718704FA7Q28511624-621163FB-4A59-497D-BD71-BCC8B17EE1F2Q28512087-3C4708A2-959D-41F8-AA94-82E95DD9F0F7Q28591717-D2BB28B9-0E87-4FE8-8FAE-4BEE211E732FQ28592236-DCE581FB-3BF5-4C71-AE5B-2AEDCC383F31Q33594773-ECE0D5BA-2D26-4D35-B62E-3070A62AC53E
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
proteinë
@sq
proteïne in Methyl CpG binding protein 2
@nl
protèin
@ace
بروتين في فأر المنازل
@ar
name
Methyl CpG binding protein 2
@en
Methyl CpG binding protein 2
@nl
type
label
Methyl CpG binding protein 2
@en
Methyl CpG binding protein 2
@nl
altLabel
Mecp2
@en
meCp-2 protein
@en
methyl-CpG-binding protein 2
@en
prefLabel
Methyl CpG binding protein 2
@en
Methyl CpG binding protein 2
@nl
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NP_001075448
XP_030107100
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ENSMUSP00000033770
ENSMUSP00000098314
ENSMUSP00000118842
ENSMUSP00000119947
ENSMUSP00000127115