SYT1

SYT1
Identifiers
AliasesSYT1, P65, SVP65, SYT, synaptotagmin 1, BAGOS
External IDsOMIM: 185605; MGI: 99667; GeneCards: SYT1
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001135805
NM_001135806
NM_001291901
NM_005639

RefSeq (protein)

NP_001129277
NP_001129278
NP_001278830
NP_005630

Location (UCSC)Chr 12: 78.86 – 79.45 MbChr 10: 108.33 – 108.85 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Synaptotagmin-1 is a protein that in humans is encoded by the SYT1 gene.

Function

Synaptotagmins are integral membrane proteins of synaptic vesicles thought to serve as sensors for calcium ions (Ca2+) in the process of vesicular trafficking and exocytosis. Calcium ion binding to synaptotagmin I participates in triggering neurotransmitter release at the synapse. [Supplied by OMIM]

SYT1 is the master switch responsible for allowing the human brain to release neurotransmitters. SYT1 senses calcium ion concentrations as low as 10 ppm and subsequently signals the SNARE complex to open fusion pores.

Interactions

SYT1 has been shown to interact with SNAP-25, STX1A and S100A13.

Clinical Significance

Mutations in the SYT1 gene cause a rare neurodevelopmental disorder known as SYT1-associated neurodevelopmental disorder (or Baker-Gordon Syndrome).