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GENATLAS PHENOTYPE

last update : 23/10/2006

Symbol	MRX14
Location	Xp11.3-q13.2
HGNC id	7243
Name	mental retardation, 14
Main clinical features	moderate-severe, with seizures, microcephaly, anteverted pinnae and macroorchidism
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, MRX15, MRX18, MRX22, MRX26, MRX31, MRX38, MRX50 (300115)