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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 05-10-2017
Symbol MRX19
Location Xp22.12
HGNC id 7248
Name mental retardation, 19
Corresponding gene RPS6KA3
Main clinical features nonspecific mental retardation, very mild mental retardation, compatible with social autonomy
Genetic determination sex linked
Function/system disorder mental retardation
Type disease
Gene product
Name growth factor regulated protein kinase, ribosomal S6 kinase, polypeptide 3,(RPS6KA3)
Remark(s)
  • overlapping with MRX24, MRX49, MRX37, MRX50