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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 23/10/2006
Symbol MRX28
Location Xq28
HGNC id 7258
Name mental retardation, 28
Corresponding gene MECP2
Main clinical features nonspecific X-linked mental retardation
Genetic determination sex linked
Function/system disorder mental retardation
Type disease
Gene product
Name methyl-CPG binding protein 2
Remark(s)
  • in the same interval than MRX3, MRXS31, MRX25, MRX41, but not mutated in GDI1