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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 27-03-2009
Symbol MRX27
Location Xq24-q26
HGNC id 7257
Name mental retardation, 27
Corresponding gene UPF3B
Main clinical features
  • nonspecific form of X-linked mental retardation, with lower verbal IQs than performance IQs
  • Genetic determination sex linked
    Function/system disorder mental retardation
    Type disease
    Mechanism(s)
    Gene mutationChromosome rearrangementEffectComments
    missense   truncated protein  
    Remark(s) in the same interval than MRX80, MRX35 and MRX23