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Phenotypes Associated with This Genotype
Genotype
MGI:8349842
Allelic
Composition
Kcnc1em1Emgol/Kcnc1+
Genetic
Background
C57BL/6J-Kcnc1em1Emgol
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kcnc1em1Emgol mutation (0 available); any Kcnc1 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• normal neonatal motor behaviors (horizontal and vertical screen, cliff avoidance, quadrupedal walking, etc.) at ages P5, P7, P9, P11, P13, and P15
• normal auditory startle reflex at ages P5, P7, P9, P11, P13, and P15
• hindlimb clasping in tail suspension test at age 6 months
• tendency to fall in ledge test at age 6 months
• unsteady gait (uncoordinated hind limb stance) in paw print analysis at age 6 months
• reduced latency to fall in accelerating rotarod test at age 6 months
• uncoordinated hind limb stance in elevated beam test at age 6 months
• spontaneous seizures from age 4 months
• accelerated PTZ-induced kindling at age P30
• seizures induced by high-frequency or high-intensity auditory stimuli at age P18-P20
• brief, mostly nonconvulsive, seizures at age 6 months

growth/size/body
N
• normal development (timing of fur appearance, shoulder and head elevation, incisor eruption, eye opening, and ear canal opening) up to age P15

nervous system
• spontaneous seizures from age 4 months
• accelerated PTZ-induced kindling at age P30
• seizures induced by high-frequency or high-intensity auditory stimuli at age P18-P20
• brief, mostly nonconvulsive, seizures at age 6 months
• broadening in cerebellar granule cells (CGCs)
• prolonged duration in cerebellar granule cells (CGCs)
• decreased maximum instantaneous and steady-state firing frequency in cerebellar granule cells (CGCs)
• less facilitation at parallel-fiber-to-Purkinje-cell synapses at age 6 months
• in cerebral cortex parvalbumin-positive GABAergic fast-spiking interneurons (PV-INs) stimulated with 20/40/120 Hz action potentials

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
progressive myoclonus epilepsy 7 DOID:0111447 OMIM:616187
J:378003


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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last database update
06/09/2026
MGI 6.24
The Jackson Laboratory