Gene

kcnt2a

ID
ZDB-GENE-130530-783
Name
potassium channel, subfamily T, member 2a
Symbol
kcnt2a Nomenclature History
Previous Names
  • kcnt2 (1)
  • zmp:0000000780 (1)
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to have intracellular sodium activated potassium channel activity and outward rectifier potassium channel activity. Predicted to be involved in potassium ion transport. Predicted to localize to integral component of membrane and plasma membrane. Human ortholog(s) of this gene implicated in early infantile epileptic encephalopathy 57. Orthologous to human KCNT2 (potassium sodium-activated channel subfamily T member 2).
Genome Resources
Note
None
Comparative Information
Expression
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
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With kcnt2a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
developmental and epileptic encephalopathy 57 Alliance Developmental and epileptic encephalopathy 57 617771
Associated With kcnt2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein Length
UniProtKB:A0A8M9PST3 1130
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations