SYN2
Sign in to saveAlso known as SYNII, Synapsin 2, synapsin II
protein-coding gene in the species Homo sapiens
Gene data
SYN2- Name
- synapsin II
- Type
- protein-coding
- Aliases
- SYNII
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. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014].
via MyGene.info
Gene · Ensembl
synapsin II
- Symbol
- SYN2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 3:12,004,325-12,192,032
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Protein SYN2 PDB 1i7l.png
Show 5 more facts
- HomoloGene ID
- 49348
- exact match
- identifiers.org/ncbigene/6854
- cytogenetic location
- 3p25.2
- genomic end
- 12192032
- genomic start
- 12004388
Sources (4)
via Wikidata · CC0