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GENATLAS PHENOTYPE

last update : 18-11-2013

Symbol	MRAR2
Location	4q26
Name	non syndromic mental retardation 2
Other name(s)	mental retardation, autosomal recessive, 1
Corresponding gene	PRSS12
Other symbol(s)	ARNSMR2, MRT1
Main clinical features	intellectual impairment, mental retardation, usually in the low or middle grade range without other clinical or laboratory manifestations
Genetic determination	autosomal recessive
Function/system disorder	mental retardation
Type	disease

Gene product

Name	neurotrypsin

Remark(s)