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GENATLAS PHENOTYPE

last update : 23/10/2006

Symbol	MRX15
Location	Xp21.1-p11.22
HGNC id	7244
Name	mental retardation, 15
Main clinical features	severe, with hypotonia in infancy
Genetic determination	sex linked
Function/system disorder	mental retardation
Type	disease

Remark(s)

overlapping with a large number of other MRX gene regions : MRX1 (309530), MRX5, MRX7, MRX8, MRX9 (309549), MRX10, MRX11, MRX12, MRX13, MRX14 (300062), MRX18, MRX22, MRX26, MRX31, MRX38, MRX50 (300115)