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Symbol
Name
ID
Kcnj11
potassium inwardly rectifying channel, subfamily J, member 11
MGI:107501
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Arthrogryposis multiplex congenita
Limb joint contracture
Contractures of the joints of the lower limbs
Muscular hypotonia
Muscular hypotonia of the trunk
Muscle weakness
Disease(s) Associated with KCNJ11
permanent neonatal diabetes mellitus
transient neonatal diabetes mellitus

Mouse Phenotypes
myoclonus
impaired skeletal muscle contractility
abnormal muscle relaxation
muscle fatigue
muscle weakness
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
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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory