Gene

kcnq3

ID
ZDB-GENE-070912-301
Name
potassium voltage-gated channel, KQT-like subfamily, member 3
Symbol
kcnq3 Nomenclature History
Previous Names
  • si:ch211-66b9.3
Type
protein_coding_gene
Location
Chr: 2 Mapping Details/Browsers
Description
Predicted to have calmodulin binding activity and delayed rectifier potassium channel activity. Involved in chemical synaptic transmission. Predicted to localize to voltage-gated potassium channel complex. Human ortholog(s) of this gene implicated in autistic disorder and benign neonatal seizures. Is expressed in central nervous system; heart; and inner ear. Orthologous to human KCNQ3 (potassium voltage-gated channel subfamily Q member 3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
4 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Chege et al., 2012
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With kcnq3 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
benign neonatal seizures Alliance Seizures, benign neonatal, 2 121201
Associated With kcnq3 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations