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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sod1tm1Dkd
targeted mutation 1, Dipak K Das
MGI:2387861
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sod1tm1Dkd/Sod1tm1Dkd involves: 129S1/Sv * 129X1/SvJ MGI:3783678


Genotype
MGI:3783678
hm1
Allelic
Composition
Sod1tm1Dkd/Sod1tm1Dkd
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sod1tm1Dkd mutation (0 available); any Sod1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• significantly higher than in controls after ischemia (J:60470)
• extent of myocardial necrosis following ischemia and reperfusion is similar to that observed in wild-type (J:89952)
• following ischemia and 30 minutes reperfusion, creatine kinase release is significantly higher from mutant hearts, and release progressively increases with reperfusion duration
• after 30 minutes of global ischemia, developed force (dF) in mutant hearts does not recover beyond 90% of baseline after 30 minutes of reperfusion
• significantly slower recovery of dF and dF/dTmax is observed in mutant hearts after 15 minutes of reperfusion
• infarct size is significantly greater relative to wild-type and heterozygous animals after 30 minutes of global ischemia

muscle
• significantly higher than in controls after ischemia (J:60470)
• extent of myocardial necrosis following ischemia and reperfusion is similar to that observed in wild-type (J:89952)
• after 30 minutes of global ischemia, developed force (dF) in mutant hearts does not recover beyond 90% of baseline after 30 minutes of reperfusion
• significantly slower recovery of dF and dF/dTmax is observed in mutant hearts after 15 minutes of reperfusion

homeostasis/metabolism
• infarct size is significantly greater relative to wild-type and heterozygous animals after 30 minutes of global ischemia

cellular
• significantly higher than in controls after ischemia (J:60470)
• extent of myocardial necrosis following ischemia and reperfusion is similar to that observed in wild-type (J:89952)
• mutant hearts produce increased amounts of hydroxyl radicals following ischemia/reperfusion
• hearts produce significantly higher amounts of malonaldehyde during the postischemic period compared to controls





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory