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FLASH GENE
Symbol SYP contributors: mct - updated : 13-11-2014
HGNC name synaptophysin
HGNC id 11506
ASSOCIATED DISORDERS
corresponding disease(s) MRX96
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
in mental retardation
Susceptibility to attention deficit hyperactivity disorder
Variant & Polymorphism SNP
  • associated to attention deficit hyperactivity disorder
  • interaction of MAOA and SYP may be involved in the genetic mechanism of ADHD-I subtype
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • mice lacking Syp, a modulator of neurotransmitter release, are defective in delaying clock phase
  • from mice 9 months old on, a progressive decrease of the presence of SYP was found under Inner hair cells and outer (OHCs) hair cells rows starting at the basal coil and reaching the apical coil in the oldest mice