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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for SYN3 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID8224
Official gene symbolSYN3
Full namesynapsin III
Aliases,-,
Gene summaryThis 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. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq]
LocationChromosome: 22   Locus: 22q12.3
Gene position33454377 - 32908539  Map Viewer
Gene orientationminus
Gene size545839 bp
Gene sequence