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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Kcnn2
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2
MGI:2153182
30 phenotypes from 13 alleles in 13 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Kcnn2bc-2J/Kcnn2bc-2J
C57BL/6J-Kcnn2bc<2J 		abnormal gait J:6710
abnormal locomotor coordination J:6710
decreased body size J:6710
impaired limb coordination J:6710
postnatal lethality, incomplete penetrance J:6710
normal reproductive system phenotype J:6710
tremors J:6710
Kcnn2bc-3J/Kcnn2bc-3J
C3H/HeSn-bc3J 		abnormal gait J:6710
abnormal locomotor coordination J:6710
decreased body size J:6710
impaired limb coordination J:6710
male infertility J:6710
preweaning lethality, incomplete penetrance J:6710
tremors J:6710
Kcnn2bc-3J/Kcnn2bc-5J
(C3H/HeSn-bc3J x LP/J-bc5J)F1 		abnormal gait J:6710, J:78381
abnormal locomotor behavior J:6710, J:78381
impaired limb coordination J:6710, J:78381
tremors J:6710, J:78381
Kcnn2bc-4J/Kcnn2bc-4J
involves: C57BL/6By 		abnormal gait J:30778
abnormal locomotor coordination J:30778
impaired limb coordination J:30778
tremors J:30778
Kcnn2bc-6J/Kcnn2bc-6J
C57BL/6J-Kcnn2bc-6J/GrsrJ 		abnormal gait J:215011
normal hearing/vestibular/ear phenotype J:215011
male infertility J:215011
tremors J:215011
normal vision/eye phenotype J:215011
Kcnn2bc-6J/Kcnn2bc-6J
involves: C57BL/6J * CAST/EiJ 		prenatal lethality, incomplete penetrance J:215011
Kcnn2bc-7J/Kcnn2bc-7J
B6.Cg-Kcnn2bc-7J/GrsrJ 		ataxia J:207676
decreased body size J:207676
normal hearing/vestibular/ear phenotype J:207676
male infertility J:207676
tremors J:207676
normal vision/eye phenotype J:207676
Kcnn2bc-8J/Kcnn2bc-8J
C57BL/6J-bc8J/GrsrJ 		ataxia J:174667
decreased body size J:174667
tremors J:174667
Kcnn2bc-9J/Kcnn2bc-9J
C57BL/6J-bc9J/GrsrJ 		ataxia J:174668
decreased body size J:174668
tremors J:174668
Kcnn2bc/Kcnn2bc
Not Specified 		abnormal gait J:136183
abnormal involuntary movement J:136183
abnormal locomotor coordination J:136183
decreased body size J:136183
impaired limb coordination J:136183
male infertility J:6710
postnatal lethality, incomplete penetrance J:136183
tremors J:136183
Kcnn2fri/Kcnn2fri
129S2.C3Pas-Kcnn2fri 		abnormal afterhyperpolarization J:177761
abnormal single cell response J:177761
decreased body size J:177761
decreased physiological sensitivity to xenobiotic J:177761
reduced male fertility J:177761
normal reproductive system phenotype J:177761
tremors J:177761
Kcnn2fri/Kcnn2fri
involves: C3H 		abnormal brain white matter morphology J:13711
abnormal gait J:70213
abnormal motor coordination/balance J:70213
abnormal short-term object recognition memory J:70213
abnormal spinal cord white matter morphology J:13711
decreased vertical activity J:70213
impaired limb coordination J:70213
short stride length J:70213
tremors J:13711, J:70213
Kcnn2m1Btlr/Kcnn2m1Btlr
C57BL/6J-Kcnn2m1Btlr 		abnormal coat appearance J:137501
abnormal gait J:137501
abnormal sexual interaction J:137501
decreased body size J:137501
hunched posture J:137501
tremors J:137501
Kcnn2tm1.1Jpad/Kcnn2tm1.1Jpad
Not Specified 		abnormal action potential J:187145
abnormal afterhyperpolarization J:94941
Kcnn2tm1Jpad/Kcnn2tm1Jpad
Not Specified 		no abnormal phenotype detected J:94941
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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04/23/2024
MGI 6.23 		The Jackson Laboratory