Gene
hcn2b
- ID
- ZDB-GENE-030131-8228
- Name
- hyperpolarization activated cyclic nucleotide-gated potassium channel 2b
- Symbol
- hcn2b Nomenclature History
- Previous Names
-
- hcn2
- si:dkey-28h18.1
- wu:fj61d07
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Description
- Predicted to enable voltage-gated potassium channel activity. Predicted to be involved in potassium ion transmembrane transport; regulation of membrane depolarization; and sodium ion transmembrane transport. Predicted to act upstream of or within potassium ion transport; sodium ion transport; and transmembrane transport. Predicted to be located in membrane. Predicted to be part of HCN channel complex. Predicted to be active in axon and dendrite. Human ortholog(s) of this gene implicated in familial febrile seizures 2. Orthologous to human HCN2 (hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Trapani et al., 2011
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 3 figures from RodrÃguez-Ortiz et al., 2021
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| familial febrile seizures 2 | Alliance | Febrile seizures, familial, 2 | 602477 |
| familial febrile seizures 2 | Alliance | Generalized epilepsy with febrile seizures plus, type 11 | 602477 |
| familial febrile seizures 2 | Alliance | {Epilepsy, idiopathic generalized, susceptibility to, 17} | 602477 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
| Protein | Length |
|---|---|
|
UniProtKB:A0A8N7T6V3
|
979 |
|
UniProtKB:A0A8M3B5M0
|
538 |
Interactions and Pathways
No data available
Plasmids
No data available