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Phenotypes Associated with This Genotype
Genotype
MGI:4420395
Allelic
Composition
Scn4atm1Ljh/Scn4a+
Genetic
Background
B6.129S4-Scn4atm1Ljh
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn4atm1Ljh mutation (0 available); any Scn4a mutation (70 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• fiber size variation and the presence of internalized nuclei are first observed at 4 months of age, becoming increasingly abnormal with age
• muscle fibers from tibialis anterior, quadriceps and gastrocnemius muscles switch from a mix of glycolytic and oxidative fibers to an increased number of oxidative fibers typical of chronic muscle activity
• twitch force elicited by direct stimulation of muscle in 8-14 month old mice is 44% of that generated by the control; in younger mice (3-5 month) twitch force is 72%
• under tetanic stimulation, kinetics of force buildup and muscle relaxation from last stimulus are prolonged (110% vs 54% and 39% vs 30%, respectively)
• tetanic force is 34% less in 8-14 months old mice during 100-Hz stimulation compared in control
• peak tetanic force under increased K+ (8mM) conditions is decreased by 46%, while control is increased by 3%
• 88% loss of force is observed under increased K+ (10 mM) conditions as compared to control (9%), in addition, lowering Ca2+ increases weakness, but does not alter recovery time
• tetanic force is further decreased by administration of ouabain (a Na+/K+ pump inhibitor) under increased K+ conditions
• robust myotonia is observed in hind limbs muscles by one month of age
• increased muscle irritability during electromyography in response to needle movement
• time to relaxation is increased by 69% following direct stimulation compared to control in 8 - 14 month old mice, however, younger (3-5 month) mice do not differ significantly from control
• under tetanic stimulation, kinetics of force buildup and muscle relaxation from last stimulus are prolonged (110% vs 54% and 39% vs 30%, respectively)
• induced fatigue of isolated extensor digitorum longus (EDL) results in delayed weakness (time required for 50% decline in force) and prolonged recovery compared to control
• mild myopathy is observed at 4 months; scattered internalized nuclei suggest regeneration by satellite cells

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hyperkalemic periodic paralysis DOID:14451 OMIM:170500
J:135831


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
04/16/2024
MGI 6.23
The Jackson Laboratory