rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
28348241
2017
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.
25818041
2015
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
T
0.800
GeneticVariation
CLINVAR
Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome.
23696494
2013
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
17296936
2007
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
T
0.800
GeneticVariation
CLINVAR
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update.
16473305
2006
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
T
0.800
GeneticVariation
CLINVAR
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome.
15057977
2004
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation.
12966522
2003
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutation analysis of the MECP2 gene in patients with Rett syndrome.
12567420
2003
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Rett syndrome in adolescent and adult females: clinical and molecular genetic findings.
12966523
2003
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation.
11738883
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein.
11283202
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome.
11376998
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
MeCP2 mutations in children with and without the phenotype of Rett syndrome.
11402105
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation.
11706982
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.
11269512
2001
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome.
10991688
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms.
11055898
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
MECP2 mutations account for most cases of typical forms of Rett syndrome.
10814719
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
10767337
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
T
0.800
GeneticVariation
CLINVAR
Reduction of mortality in specific-pathogen-free layer chickens by a caprine serum fraction after infection with Pasteurella multocida.
11055848
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
T
0.800
GeneticVariation
CLINVAR
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
10767337
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutation screening in Rett syndrome patients.
10745042
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome.
10944854
2000
rs61751443
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Rett Syndrome
0.800
GeneticVariation
UNIPROT
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome.
10991689
2000