Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10814
Gene name Gene Name - the full gene name approved by the HGNC.
Complexin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CPLX2
Synonyms (NCBI Gene) Gene synonyms aliases
921-L, CPX-2, CPX2, Hfb1
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q35.2
Summary Summary of gene provided in NCBI Entrez Gene.
Proteins encoded by the complexin/synaphin gene family are cytosolic proteins that function in synaptic vesicle exocytosis. These proteins bind syntaxin, part of the SNAP receptor. The protein product of this gene binds to the SNAP receptor complex and di
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT713799 hsa-miR-574-3p HITS-CLIP 19536157
MIRT713798 hsa-miR-1306-5p HITS-CLIP 19536157
MIRT713797 hsa-miR-3622a-3p HITS-CLIP 19536157
MIRT713796 hsa-miR-3622b-3p HITS-CLIP 19536157
MIRT713795 hsa-miR-6765-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000149 Function SNARE binding IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0005829 Component Cytosol IEA
GO:0006904 Process Vesicle docking involved in exocytosis TAS 7553862
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605033 2310 ENSG00000145920
Protein
UniProt ID Q6PUV4
Protein name Complexin-2 (Complexin II) (CPX II) (Synaphin-1)
Protein function Negatively regulates the formation of synaptic vesicle clustering at active zone to the presynaptic membrane in postmitotic neurons. Positively regulates a late step in exocytosis of various cytoplasmic vesicles, such as synaptic vesicles and ot
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05835 Synaphin 1 133 Synaphin protein Family
Tissue specificity TISSUE SPECIFICITY: Nervous system. In hippocampus and cerebellum, expressed mainly by excitatory neurons. Down-regulated in brain cortex from patients suffering from Huntington disease, bipolar disorder or major depression. Down-regulated in cerebellum f
Sequence
Sequence length 134
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Synaptic vesicle cycle  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019 23527680
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
14708030, 11483314
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder 20584925 ClinVar
Myocardial infarction Myocardial Infarction 21211798 ClinVar
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Inhibit 31699905
Atrophy Associate 22832958
Brain Diseases Associate 25297695
Brain Injuries Traumatic Associate 25297695
Breast Neoplasms Associate 36581948
Carcinoma Neuroendocrine Associate 28239029
Cognition Disorders Associate 25297695
COVID 19 Associate 34185889
Cushing's symphalangism Stimulate 23912489
Dementia Inhibit 22832958