×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
10508514
1999
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
12615169
2003
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study.
27354166
2016
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2.
8177735
1993
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Functional consequences of Rett syndrome mutations on human MeCP2.
11058114
2000
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.
16169931
2006
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
The MSL complex: juggling RNA-protein interactions for dosage compensation and beyond.
25900149
2015
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Prevalence and architecture of de novo mutations in developmental disorders.
28135719
2017
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Using a large international sample to investigate epilepsy in Rett syndrome.
23421866
2013
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
The MRG domain mediates the functional integration of MSL3 into the dosage compensation complex.
15988010
2005
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
MECP2 mutations in males.
17351020
2007
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion.
15558314
2005
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
17267601
2007
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Rett syndrome: revised diagnostic criteria and nomenclature.
21154482
2010
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
MECP2 duplication: possible cause of severe phenotype in females.
24458799
2014
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16.
16227571
2005
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Epilepsy in a representative series of Rett syndrome.
11227330
2001
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Structural and biochemical studies on the chromo-barrel domain of male specific lethal 3 (MSL3) reveal a binding preference for mono- or dimethyllysine 20 on histone H4.
20943666
2010
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome.
15057977
2004
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Male Rett phenotypes in T158M and R294X MeCP2-mutations.
17236109
2006
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Mof-associated complexes have overlapping and unique roles in regulating pluripotency in embryonic stem cells and during differentiation.
24898753
2014
×
Entrez Id:
10943
Gene Symbol:
MSL3
MSL3
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Corecognition of DNA and a methylated histone tail by the MSL3 chromodomain.
20657587
2010
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
18337588
2008
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
24399845
2014
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Muscle hypotonia
0.400
GeneticVariation
CLINVAR
Early progressive encephalopathy in boys and MECP2 mutations.
16832102
2006