Symbol
Name
ID

Kcnj11
potassium inwardly rectifying channel, subfamily J, member 11
MGI:107501

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Hypoglycemic seizures

Peripheral neuropathy

Hypsarrhythmia

Apraxia

Coma

Hypoglycemic coma

Intellectual disability

Global developmental delay

Motor delay

Seizures

Generalized myoclonic seizures

Generalized tonic-clonic seizures

Disease(s) Associated with KCNJ11

hyperinsulinemic hypoglycemia

permanent neonatal diabetes mellitus

transient neonatal diabetes mellitus

Mouse Phenotypes		convulsive seizures	myoclonus	tonic-clonic seizures	abnormal nervous system electrophysiology	abnormal action potential	abnormal nerve fiber response	abnormal nerve fiber response intensity	abnormal channel response
Availability	Mouse Genotype	convulsive seizures	myoclonus	tonic-clonic seizures	abnormal nervous system electrophysiology	abnormal action potential	abnormal nerve fiber response	abnormal nerve fiber response intensity	abnormal channel response
	Kcnj11^tm1Sse/Kcnj11^tm1Sse
	Gt(ROSA)26Sor^{tm1(Kcnj11*V59M)Fmas}/Gt(ROSA)26Sor⁺ Tg(Nes-cre)1Kln/0 (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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