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Symbol
Name
ID

Kcnq5
potassium voltage-gated channel, subfamily Q, member 5
MGI:1924937

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Brain atrophy	Absent speech	Delayed speech and language development	Intellectual disability	Unsteady gait	Epileptic encephalopathy	Global developmental delay	Seizure	Focal impaired awareness seizure	Infantile spasms	Tonic seizure
Disease(s) Associated with KCNQ5
autosomal dominant intellectual developmental disorder 46

Mouse Phenotypes		abnormal afterhyperpolarization
Availability	Mouse Genotype	abnormal afterhyperpolarization
	Kcnq5^tm1.1Tjj/Kcnq5^tm1.1Tjj

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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