Gene
kcnq2b
- ID
- ZDB-GENE-120130-1
- Name
- potassium voltage-gated channel, KQT-like subfamily, member 2b
- Symbol
- kcnq2b Nomenclature History
- Previous Names
-
- si:ch211-158n11.6
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have delayed rectifier potassium channel activity. Predicted to be involved in potassium ion transmembrane transport. Predicted to localize to several cellular components, including dendrite membrane; neuronal cell body membrane; and voltage-gated potassium channel complex. Is expressed in brain; heart; and inner ear.
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- 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 |
|---|---|---|---|
| benign neonatal seizures | Alliance | Myokymia | 121200 |
| benign neonatal seizures | Alliance | Seizures, benign neonatal, 1 | 121200 |
| developmental and epileptic encephalopathy 7 | Alliance | Developmental and epileptic encephalopathy 7 | 613720 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
kcnq2b-202
(1)
|
Havana | 4819 nt |
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance