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GENATLAS PHENOTYPE

last update : 06-10-2017

Symbol	MRX63
Location	Xq23
HGNC id	7297
Name	mental retardation, 63
Corresponding gene	ACSL4
Other symbol(s)	MRX68
Main clinical features	nonspecific, non progressive mental retardation ranging from severe to moderate, without seizures, whereas carrier females showed highly variable cognitive capacities, ranging from moderate mental retardation to normal intelligence same as MRX68
Genetic determination	sex linked
Function/system disorder	mental retardation
Type	disease

Gene product

Name	fatty acid CoA ligase 4

Remark(s)