Symbol
Name
ID

Kcnq3
potassium voltage-gated channel, subfamily Q, member 3
MGI:1336181

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

EEG abnormality

Abnormal nonverbal communicative behavior

Delayed speech and language development

Lack of spontaneous play

Impaired ability to form peer relationships

Autism

Inflexible adherence to routines

Motor stereotypy

Restrictive behavior

Intellectual disability

Myokymia

Global developmental delay

Motor delay

Seizure

Bilateral tonic-clonic seizure

Focal clonic seizure

Febrile seizure (within the age range of 3 months to 6 years)

Disease(s) Associated with KCNQ3

autistic disorder

benign neonatal seizures

Mouse Phenotypes		nervous system phenotype	seizures	abnormal seizure response to electrical stimulation	abnormal hippocampus morphology	astrocytosis	abnormal nervous system electrophysiology	abnormal afterhyperpolarization	abnormal neuron physiology
Availability	Mouse Genotype	nervous system phenotype	seizures	abnormal seizure response to electrical stimulation	abnormal hippocampus morphology	astrocytosis	abnormal nervous system electrophysiology	abnormal afterhyperpolarization	abnormal neuron physiology
	Kcnq3^tm1.1Naas/Kcnq3^tm1.1Naas	*
	Kcnq3^tm1Dgen/Kcnq3^tm1Dgen
	Kcnq3^tm1.1Naas/Kcnq3⁺
	Emx1^tm1(cre)Krj/? Kcnq3^tm1.1Avtz/Kcnq3^tm1.1Avtz (conditional)

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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