Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn5atm1(SCN5A)Rdn mutation
(1 available);
any
Scn5a mutation
(104 available)
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normal phenotype
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• homozygotes are viable, exhibit no obvious morphological abnormalities and are fertile, and have normal sodium channel function as shown by electrocardiograms, ventricular myocyte action potentials, and ventricular myocyte sodium currents
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cardiovascular system
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• intermediate at 12 weeks
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• intermediate at 12 weeks
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• intermediate at 3 weeks
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• intermediate at 3 and 12 weeks
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• intermediate at 3 weeks
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muscle
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• intermediate at 12 weeks
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