rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
17296936
2007
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
A novel familial MECP2 mutation in a young boy: clinical and molecular findings.
16966553
2006
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
12615169
2003
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome.
11885030
2002
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
12325019
2002
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
A Rett syndrome MECP2 mutation that causes mental retardation in men.
11805248
2002
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.
12161600
2002
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
MECP2 is highly mutated in X-linked mental retardation.
11309367
2001
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
MECP2 mutation in male patients with non-specific X-linked mental retardation.
11007980
2000
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
0.800
GeneticVariation
UNIPROT
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males.
10986043
2000
rs28934908
×
Entrez Id:
4204
Gene Symbol:
MECP2
MECP2
Mental Retardation, X-Linked, Syndromic 13
A
0.800
CausalMutation
CLINVAR