Deletion of SYN3 was found to alter social behavior in male mice (Greco et al., 2013).
Molecular Function
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases.
External Links
References
Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Autism-related behavioral abnormalities in synapsin knockout mice.
Model Type:
Genetic
Model Genotype:
Homozygous
Mutation:
2.0 kb XhoISstI fragment containing exon 1 was replaced by a neomycin resistance gene in reverse orientation.
Allele Type: Knockout
Strain of Origin: Not specified
Genetic Background: C57BL/6J
ES Cell Line: RW4
Mutant ES Cell Line: Not Specified
Model Source: Greengard laboratory (PMID 12040043)
Model Type:
Genetic
Model Genotype:
Heterozygous
Mutation:
Gene trap mediated deletion of exon 1 of Syn3 gene.
Allele Type: Knockout
Strain of Origin: Not specified
Genetic Background: C57BL/6J
ES Cell Line: RW4
Mutant ES Cell Line: Not Specified
Model Source: Greengard laboratory (PMID 12040043)
Description: Decreased aggression indicated by reduced social interaction with intruder after 1-2 months of social isolation
Exp Paradigm: Resident intruder test
Description: Decreased social novelty indicated by failure to discirminate between familiar vs. novel mouse
Exp Paradigm: Social novelty phase of three-chambered social approach test
Description: Decreased social interaction demonstrated by virtually absent significant food preference
Exp Paradigm: Social transmission of food preference task