| STXBP1 | 
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| Identifiers | 
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| Aliases | STXBP1, MUNC18-1, NSEC1, P67, RBSEC1, UNC18, syntaxin binding protein 1 | 
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| External IDs | OMIM: 602926; MGI: 107363; HomoloGene: 2382; GeneCards: STXBP1; OMA:STXBP1 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 2 (mouse) | 
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 |  |  | Band | 2 B|2 22.09 cM | Start | 32,677,614 bp | 
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 | End | 32,737,257 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | middle temporal gyrus
 lateral nuclear group of thalamus
 Brodmann area 23
 Pons
 superior frontal gyrus
 primary visual cortex
 right hemisphere of cerebellum
 pars compacta
 postcentral gyrus
 paraflocculus of cerebellum
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 | | Top expressed in |  | neural layer of retina
 pontine nuclei
 inferior colliculi
 perirhinal cortex
 superior colliculus
 central gray substance of midbrain
 piriform cortex
 Medulla Oblongata
 cerebellar cortex
 medial vestibular nucleus
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Syntaxin-binding protein 1 (also known as Munc18-1) is a protein that in humans is encoded by the STXBP1 gene. This gene encodes a syntaxin-binding protein. The encoded protein appears to play a role in release of neurotransmitters via regulation of syntaxin, a transmembrane attachment protein receptor. Mutations in this gene have been associated with neurological disorders including epilepsy, intellectual disability, and movement disorders.