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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 05-10-2017
Symbol MRX58
Location Xp11.4
HGNC id 7291
Name mental retardation, 58
Corresponding gene TSPAN7
Main clinical features
  • nonsyndromic X-linked mental retardation with mild to moderate mental retardation and no consistent dysmorphic features, and obligatory carrier females normal
  • Genetic determination sex linked
    Function/system disorder mental retardation
    Type disease
    Gene product
    Name tetraspanin 7
    Remark(s)