VAMP2
Sign in to saveAlso known as SYB2, VAMP-2, vesicle associated membrane protein 2, NEDHAHM
gen de la especie Homo sapiens
In the Vinony graph
Within Vinony's link graph, VAMP2 is referenced by 87 other articles, and connects out to COPII, AP-type membrane coat adaptor complex and PubMed.
It is catalogued under topics including Genes on human chromosome 17 and Neural synapse.
Its subject is documented across 4 Wikipedia language editions.
Gene data
VAMP2- Name
- vesicle associated membrane protein 2
- Type
- protein-coding
- Position
- 8,159,149–8,163,584 (−)
- Aliases
- NEDHAHM, SYB2, VAMP-2
- Ensembl
- ENSG00000220205
- RefSeq RNA
- NM_001330125.1, NM_014232.3
- RefSeq protein
- NP_001317054.1, NP_055047.2
The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Synaptobrevins/VAMPs, syntaxins, and the 25-kD synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. This gene is thought to participate in neurotransmitter release at a step between docking and fusion. The protein forms a stable complex with syntaxin, synaptosomal-associated protein, 25 kD, and synaptotagmin. It also forms a distinct complex with synaptophysin. It is a likely candidate gene for familial infantile myasthenia (FIMG) because of its map location and because it encodes a synaptic vesicle protein of the type that has been implicated in the pathogenesis of FIMG. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
vesicle associated membrane protein 2
- Symbol
- VAMP2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 17:8,159,149-8,163,584
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Three-dimensional structure of the complexin SNARE complex - Vesicle-associated membrane protein 2 1KIL.png
Show 8 more facts
- HomoloGene ID
- 7591
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/6844
- genomic end
- 8066864
- genomic start
- 8062467
- chromosome
- human chromosome 17
- cytogenetic location
- 17p13.1
- expressed in
- anterior pituitary
Sources (3)
via Wikidata · CC0