ZFIN is now using GRCz12tu for Genomic Data
        
        
        Gene
syt1b
- ID
- ZDB-GENE-060503-166
- Name
- synaptotagmin Ib
- Symbol
- syt1b Nomenclature History
- Previous Names
- 
    
        
    
    
        
        - si:dkey-30c15.14 (1)
 
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Genome Assembly
- GRCz12tu
- Annotation Status
- Current
- Description
- Predicted to enable SNARE binding activity; calcium ion sensor activity; and calcium-dependent phospholipid binding activity. Predicted to be involved in calcium-dependent activation of synaptic vesicle fusion; regulation of calcium ion-dependent exocytosis; and regulation of synaptic vesicle exocytosis. Predicted to be located in chromaffin granule membrane and synapse. Predicted to be active in axon; plasma membrane; and secretory vesicle. Is expressed in brain. Orthologous to human SYT1 (synaptotagmin 1).
- Genome Resources
- Note
- None
- Comparative Information
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- All Expression Data
- 2 figures from Henry et al., 2021
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
                
                    
                        Wild Type Expression Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    - All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
                
                    
                        Phenotype Summary
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Mutations
                    
                    
                
                
            
        
        
    
        
            
            
    
    
                
                    
                        Human Disease
                    
                    
                
                
            
        
        
    
        
            
            
    
    | Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID | 
|---|---|---|---|
| Baker-Gordon syndrome | 618218 | 
                
                    
                        Domain, Family, and Site Summary
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    
    
    
            
        
    
    
    
                
                    
                        Domain Details Per Protein
                    
                    
                
                
            
        
        
    
        
            
                
    
        
    | Protein | Additional Resources | Length | C2 domain | C2 domain superfamily | Synaptotagmin | 
|---|---|---|---|---|---|
| UniProtKB:A3KQ92 | InterPro | 388 | |||
| UniProtKB:A0A8M9PPX1 | InterPro | 380 | 
- Genome Browsers
                
                    
                        Interactions and Pathways
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    
                
                    
                        Plasmids
                    
                    
                
                
            
        
        
    
        
            
            
    
    
        
    
No data available
    
        
        
    
    
    - Genome Browsers
