Gene Gene information from NCBI Gene database.
Entrez ID 6854
Gene name Synapsin II
Gene symbol SYN2
Synonyms (NCBI Gene)
SYNII
Chromosome 3
Chromosome location 3p25.2
Summary This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptog
miRNA miRNA information provided by mirtarbase database.
66
miRTarBase ID miRNA Experiments Reference
MIRT1405397 hsa-miR-1 CLIP-seq
MIRT1405398 hsa-miR-206 CLIP-seq
MIRT1405399 hsa-miR-3121-3p CLIP-seq
MIRT1405400 hsa-miR-3190 CLIP-seq
MIRT1405401 hsa-miR-3202 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
2
Transcription factor Regulation Reference
EGR1 Unknown 7592648
ETV4 Unknown 7592648
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 23406870, 33961781
GO:0005524 Function ATP binding IEA
GO:0005524 Function ATP binding TAS 15217342
GO:0005886 Component Plasma membrane IEA
GO:0007268 Process Chemical synaptic transmission IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600755 11495 ENSG00000157152
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q92777
Protein name Synapsin-2 (Synapsin II)
Protein function Neuronal phosphoprotein that coats synaptic vesicles, binds to the cytoskeleton, and is believed to function in the regulation of neurotransmitter release. May play a role in noradrenaline secretion by sympathetic neurons (By similarity). {ECO:0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10581 Synapsin_N 2 39 Synapsin N-terminal Domain
PF02078 Synapsin 111 212 Synapsin, N-terminal domain Domain
PF02750 Synapsin_C 214 416 Synapsin, ATP binding domain Domain
Tissue specificity TISSUE SPECIFICITY: Central and peripheral nervous systems.
Sequence
MMNFLRRRLSDSSFIANLPNGYMTDLQRPEPQQPPPPPPPGPGAASASAAPPTASPGPER
RPPPASAPAPQPAPTPSVGSSFFSSLSQAVKQTAASAGLVDAPAPAPAAARKAKVLLVVD
EPHADWAKCFRGKKVLGDYDIKVEQAEFSELNLVAHADGTYAVDMQVLRNGTKVVRSFRP
DFVLIRQHAFGMAENEDFRHLIIGMQYAGLPS
INSLESIYNFCDKPWVFAQLVAIYKTLG
GEKFPLIEQTYYPNHKEMLTLPTFPVVVKIGHAHSGMGKVKVENHYDFQDIASVVALTQT
YATAEPFIDSKYDIRVQKIGNNYKAYMRTSISGNWKTNTGSAMLEQIAMSDRYKLWVDTC
SEMFGGLDICAVKAVHGKDGKDYIFEVMDCSMPLIGEHQVEDRQLITELVISKMNQ
LLSR
TPALSPQRPLTTQQPQSGTLKDPDSSKTPPQRPPPQGGPGQPQGMQPPGKVLPPRRLPPG
PSLPPSSSSSSSSSSSAPQRPGGPTTHGDAPSSSSSLAEAQPPLAAPPQKPQPHPQLNKS
QSLTNAFSFSESSFFRSSANEDEAKAETIRSLRKSFASLFSD
Sequence length 582
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Serotonin Neurotransmitter Release Cycle
Dopamine Neurotransmitter Release Cycle
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Schizophrenia Uncertain significance rs2470279573 RCV002289042
SYN2-related disorder Benign; Uncertain significance; Likely benign rs794999, rs2470236042, rs310764, rs151063425, rs191537003, rs544852588, rs750769489, rs749315558 RCV003984085
RCV003896493
RCV003974701
RCV003964154
RCV003941424
RCV003922245
RCV003934152
RCV003954394
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 39650656
Bipolar Disorder Associate 22384280, 27515700
Bone Diseases Metabolic Associate 29763751
COVID 19 Associate 34299101
Depressive Disorder Major Associate 27515700
Diabetes Mellitus Type 2 Associate 21084393, 32948839
Epilepsy Associate 22571925
Mental Disorders Associate 22571925
Mood Disorders Associate 27515700
Mucocutaneous Lymph Node Syndrome Associate 37894766