Gene
kcnk9
- ID
- ZDB-GENE-070705-260
- Name
- potassium channel, subfamily K, member 9
- Symbol
- kcnk9 Nomenclature History
- Previous Names
-
- si:ch211-268f14.1
- si:ct583670.1
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to have potassium ion leak channel activity. Predicted to be involved in potassium ion transmembrane transport and stabilization of membrane potential. Predicted to localize to integral component of plasma membrane. Human ortholog(s) of this gene implicated in Birk-Barel syndrome. Orthologous to human KCNK9 (potassium two pore domain channel subfamily K member 9).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Skarsfeldt et al., 2018
- 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 |
|---|---|---|---|
| Birk-Barel syndrome | Alliance | Birk-Barel syndrome | 612292 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Potassium channel domain | Potassium channel subfamily K member 9 | Two pore domain potassium channel | Two pore domain potassium channel, TASK family |
|---|---|---|---|---|---|
|
UniProtKB:A0A8M1NHJ6
|
399 |
Interactions and Pathways
No data available
Plasmids