Gene
kcnt2a
- ID
- ZDB-GENE-130530-783
- Name
- potassium channel, subfamily T, member 2a
- Symbol
- kcnt2a Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 2 Mapping Details/Browsers
- Description
- Is expressed in brain; neural tube; otic vesicle; and tegmentum. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 57. Orthologous to human KCNT2 (potassium sodium-activated channel subfamily T member 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Silic 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 |
|---|---|---|---|
| developmental and epileptic encephalopathy 57 | Alliance | Developmental and epileptic encephalopathy 57 | 617771 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | Calcium-activated potassium channel BK, alpha subunit | Calcium-activated potassium channel slowpoke-like | Potassium channel domain |
|---|---|---|---|---|---|
| UniProtKB:A0AB32T3C7 | InterPro | 1111 |
Interactions and Pathways
No data available
Plasmids
- Comparative Orthology
- Alliance