Symbol
| SYP
| contributors: mct - updated : 13-11-2014
|
HGNC name
| synaptophysin
|
HGNC id
| 11506
|
corresponding disease(s)
|
MRX96
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein 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
| | | |
| 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 |