Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person UniProt:O14810 CPLX1

Class:IdReferenceGeneProduct:210434
_chainChangeLogchain:1-134 added on Fri February 6 2015
_displayNameUniProt:O14810 CPLX1
_timestamp2024-11-03 19:50:34
chainchain:1-134
checksumA7A52F17F10D28A4
commentFUNCTION Positively regulates a late step in exocytosis of various cytoplasmic vesicles, such as synaptic vesicles and other secretory vesicles (PubMed:21785414). Organizes the SNAREs into a cross-linked zigzag topology that, when interposed between the vesicle and plasma membranes, is incompatible with fusion, thereby preventing SNAREs from releasing neurotransmitters until an action potential arrives at the synapse (PubMed:21785414). Also involved in glucose-induced secretion of insulin by pancreatic beta-cells. Essential for motor behavior.SUBUNIT Binds to the SNARE core complex containing SNAP25, VAMP2 and STX1A.INTERACTION Enriched at synaptic-releasing sites in mature neurons.TISSUE SPECIFICITY Nervous system. In hippocampus and cerebellum, expressed mainly by inhibitory neurons. Overexpressed in substantia nigra from patients with Parkinson disease.DISEASE The disease is caused by variants affecting the gene represented in this entry.SIMILARITY Belongs to the complexin/synaphin family.
created[InstanceEdit:210485] 2008-01-14 10:59:03
descriptionrecommendedName: Complexin-1 alternativeName: Complexin I shortName: CPX I alternativeName: Synaphin-2
geneNameCPLX1
identifierO14810
isSequenceChangedFALSE
keyword3D-structure
Cell projection
Coiled coil
Cytoplasm
Disease variant
Epilepsy
Exocytosis
Neurotransmitter transport
Proteomics identification
Reference proteome
Synapse
Transport
modified[InstanceEdit:9836292] Weiser, Joel, 2023-05-25
[InstanceEdit:9852000] Weiser, Joel, 2023-11-03
[InstanceEdit:9926675] Weiser, Joel, 2024-11-03
nameCPLX1
referenceDatabase[ReferenceDatabase:2] UniProt
referenceGene[ReferenceDNASequence:8987755] ENSEMBL:ENSG00000168993 CPLX1 [Homo sapiens]
secondaryIdentifierCPLX1_HUMAN
A6NI80
B2R4R5
D3DVN3
F1T0G1
sequenceLength134
species[Species:48887] Homo sapiens
(referenceEntity)[EntityWithAccessionedSequence:210385] CPLX1 [cytosol] [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by UniProt:O14810 CPLX1 (210434)