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References OMIM Gene GeneReviews HGMD HGNC
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)