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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
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
Kcnj11tm1Sse/Kcnj11tm1Sse
Gt(ROSA)26Sortm1(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
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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory