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
- Predicted to act upstream of or within potassium ion transport. Predicted to be located in membrane. 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
No data available
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 |
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Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Interactions and Pathways
No data available
Plasmids
No data available
Relationship | Marker Type | Marker | Accession Numbers | Citations |
---|---|---|---|---|
Contained in | BAC | DKEY-245G22 | ZFIN Curated Data |
1 - 1 of 1
Show
Type | Accession # | Sequence | Length (nt/aa) | Analysis |
---|---|---|---|---|
RNA | RefSeq:XM_068213585 (1) | 3864 nt | ||
Genomic | GenBank:CR376724 (1) | 168441 nt | ||
Polypeptide | RefSeq:XP_068069686 (1) |
- Comparative Orthology
- Alliance