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Symbol
Name
ID
Kcnq1
potassium voltage-gated channel, subfamily Q, member 1
MGI:108083
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Fatigue
Chest pain
Disease(s) Associated with KCNQ1
familial atrial fibrillation

Mouse Phenotypes
behavior/neurological phenotype
abnormal motor capabilities/coordination/movement
absent pinna reflex
impaired righting response
opisthotonus
tremors
impaired balance
impaired coordination
impaired swimming
jerky movement
head bobbing
head tossing
abnormal gait
retropulsion
hyperactivity
stereotypic behavior
circling
bidirectional circling
spinning
Availability Mouse Genotype
Kcnq1tm1Apf/Kcnq1tm1Apf
Kcnq1tm1Kpfe/Kcnq1tm1Kpfe
Kcnq1tm2Kpfe/Kcnq1tm2Kpfe
Kcnq1tm3Kpfe/Kcnq1tm3Kpfe *
Kcnq1vtg-2J/Kcnq1vtg-2J
Kcnq1vtg-3J/Kcnq1vtg-3J
Kcnq1vtg-4J/Kcnq1vtg-4J
Kcnq1m1Anu/?

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/14/2024
MGI 6.23
The Jackson Laboratory