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GENATLAS PHENOTYPE
last update : 4/09/2006
Symbol FASPS2
Location 17q25
Name familial advanced sleep phase syndrome 2
Corresponding gene CSNK1D
Main clinical features
  • mendelian circadian rhythm variant characterized by early sleep times and early-morning awakening
    • Genetic determination autosomal dominant
    Function/system disorder neurology
    Type disease
    Gene product
    Name casein kinase 1, delta
    Mechanism(s)
    Gene mutationChromosome rearrangementEffectComments
    missense   abnormal protein/loss of function T44A