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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	Peripheral neuropathy	Hypsarrhythmia	Apraxia	Coma	Intellectual disability	Global developmental delay	Motor delay	Seizures	Generalized myoclonic seizures	Generalized tonic-clonic seizures
Disease(s) Associated with KCNJ11	Peripheral neuropathy	Hypsarrhythmia	Apraxia	Coma	Intellectual disability	Global developmental delay	Motor delay	Seizures	Generalized myoclonic seizures	Generalized tonic-clonic seizures
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
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support.	last database update 10/09/2018 MGI 6.12