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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kcnj6
potassium inwardly-rectifying channel, subfamily J, member 6
MGI:104781
9 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Kcnj6tm1Stf/Kcnj6tm1Stf
Kcnj9tm1Kwn/Kcnj9tm1Kwn
involves: 129S1/Sv * 129X1/SvJ
abnormal synaptic transmission J:77047
premature death J:77047
seizures J:77047
Tg(CEPHY152F7)12Hgc/0
(C57BL/6 x FVB/N)F1
abnormal spatial learning J:128896
hypoactivity J:128896
normal nervous system phenotype J:128896
Tg(CEPHY152F7)12Hgc/0
FVB-Tg(CEPHY152F7)12Hgc
abnormal emotion/affect behavior J:128896
abnormal reflex J:128896
Tg(CEPHY152F7)57Hgc/0
(C57BL/6 x FVB/N)F1
abnormal spatial learning J:128896
hypoactivity J:128896
normal nervous system phenotype J:128896
Tg(CEPHY152F7)57Hgc/0
FVB-Tg(CEPHY152F7)57Hgc
abnormal emotion/affect behavior J:128896
abnormal reflex J:128896
Tg(CEPHY285E6)67Hgc/0
(C57BL/6 x FVB/N)F1
normal behavior/neurological phenotype J:128896
Tg(CEPHY285E6)84Hgc/0
(C57BL/6 x FVB/N)F1
normal behavior/neurological phenotype J:128896

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory