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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm
transgene insertion 5-313, Mani S Mahadevan
MGI:3813454
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Nkx2-5tm6Rph/Nkx2-5+
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0
involves: 129S1/Sv * FVB/N MGI:3813456
cx2
Nkx2-5tm6Rph/Nkx2-5+
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/Tg(DMPK/tetO-EGFP/DMPK)5-313Masm
involves: 129S1/Sv * FVB/N MGI:3813457
tg3
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0 involves: FVB/N MGI:3813458


Genotype
MGI:3813456
cx1
Allelic
Composition
Nkx2-5tm6Rph/Nkx2-5+
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nkx2-5tm6Rph mutation (0 available); any Nkx2-5 mutation (21 available)
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• by 3 weeks of treatment with doxycycline, mice exhibit myotonia

cardiovascular system
• at 2 weeks post treatment with doxycycline, mice exhibit a less dramatic increase in PR intervals than in Tg(DMPK/tetO-GFP/DMPK)5-313Masm mice




Genotype
MGI:3813457
cx2
Allelic
Composition
Nkx2-5tm6Rph/Nkx2-5+
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/Tg(DMPK/tetO-EGFP/DMPK)5-313Masm
Genetic
Background
involves: 129S1/Sv * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nkx2-5tm6Rph mutation (0 available); any Nkx2-5 mutation (21 available)
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• within 2 weeks of treatment with doxycycline, mice develop myotonia

cardiovascular system
• within 2 weeks of treatment with doxycycline, mice develop progressive heart block




Genotype
MGI:3813458
tg3
Allelic
Composition
Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit muscle fiber atrophy
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit muscles with a greater degree of fiber size variability
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit muscles with an increase in centrally nucleated fibers
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit an increase in myotonic dystrophy disease severity compared to mice treated with doxycycline starting at 2 months of age for a total of 8 weeks, showing a PR interval increase of 46.75% compared to 17.93% in the adult-induced mice, worse myotonia score, and more severe loss of grip strength, although a slightly milder muscle histology
• following treatment with doxycycline, mice exhibit myotonia (J:131302)
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit weak and intermittent myotonia at 2 weeks of age that increases in severity by 4 weeks of age (J:207560)

cardiovascular system
• following treatment with doxycycline, mice develop progressive heart block
• following treatment with doxycycline (J:131302)
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth exhibit a lengthened PR interval by 4 and 6 weeks of age, indicating cardiac conduction defects (J:207560)

behavior/neurological
• mice treated with doxycycline throughout gestation, birth, and rearing up to 6 weeks after birth have weaker forelimb grip strength at 4 and 6 weeks of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
myotonic dystrophy type 1 DOID:11722 OMIM:160900
J:207560





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last database update
08/02/2024
MGI 6.24
The Jackson Laboratory