Gene
syt2a
- ID
- ZDB-GENE-060503-315
- Name
- synaptotagmin IIa
- Symbol
- syt2a Nomenclature History
- Previous Names
-
- si:ch211-236j4.1 (1)
- Type
- protein_coding_gene
- Location
- Chr: 23 Mapping Details/Browsers
- Description
- Predicted to have several functions, including calcium ion binding activity; phospholipid binding activity; and syntaxin binding activity. Predicted to be involved in cellular response to calcium ion; regulation of secretion by cell; and synaptic vesicle cycle. Predicted to localize to axon; plasma membrane; and secretory vesicle. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome 7. Orthologous to human SYT2 (synaptotagmin 2).
- Genome Resources
- Note
- None
- All Expression Data
- Fig. 2 from Kiesow et al., 2015
- Cross-Species Comparison
- High Throughput Data
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 |
|---|---|---|---|
| congenital myasthenic syndrome 7 | Alliance | Myasthenic syndrome, congenital, 7, presynaptic | 616040 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | C2 domain | C2 domain superfamily | Synaptotagmin | Synaptotagmin 1 |
|---|---|---|---|---|---|
|
UniProtKB:F1R5C0
|
430 |
Interactions and Pathways
No data available
Plasmids
No data available