Symbol Name ID |
Kcnj11
potassium inwardly rectifying channel, subfamily J, member 11 MGI:107501 |
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 |
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Availability | Mouse Genotype | ||||||||
Kcnj11tm1Sse/Kcnj11tm1Sse | |||||||||
Gt(ROSA)26Sortm1(Kcnj11*V59M)Fmas/Gt(ROSA)26Sor+ Tg(Nes-cre)1Kln/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 04/03/2018 MGI 6.11 |
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