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GENATLAS PHENOTYPE

last update : 10-01-2009

Symbol	MRX13
Location	Xp21.22-q22.3
HGNC id	7242
Name	mental retardation, 13
Main clinical features	isolated mental retardation, non syndromic
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, MRX14 (300062), MRX15, MRX18, MRX22, MRX26, MRX31, MRX38, MRX50 (300115)