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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(APOC3)3707Bres
transgene insertion 3707, Jan L Breslow
MGI:3703618
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Ldlrtm1Her/Ldlrtm1Her
Tg(APOC3)3707Bres/?
involves: 129S7/SvEvBrd * C57BL/6J * CBA/J MGI:4367083
cx2
Ldlrtm1Her/Ldlrtm1Her
Tg(APOC3)3707Bres/?
Tg(Mt1-CETP)#Tall/?
involves: 129S7/SvEvBrd * C57BL/6J * CBA/J MGI:4941579
tg3
Tg(APOC3)3707Bres/0 involves: C57BL/6J * CBA/J MGI:3710973


Genotype
MGI:4367083
cx1
Allelic
Composition
Ldlrtm1Her/Ldlrtm1Her
Tg(APOC3)3707Bres/?
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ldlrtm1Her mutation (19 available); any Ldlr mutation (76 available)
Tg(APOC3)3707Bres mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• DL-LDL levels increased about 2 fold over the 32mg/dl level found in mice carrying only the transgene
• 3-4 fold increase in IDL-LDL on a Western diet over the 86mg/dl level found in mice carrying only the transgene but also on a Western diet
• increased 10 fold over the level of 50mg/dl or less found in mice carrying only the transgene
• more pronounced increase when fed a Western diet

cardiovascular system
• lesions at the base of the aorta are 2-3 times the size of lesions in mice lacking the transgene but homozygous for Ldlr deficiency

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
familial combined hyperlipidemia DOID:13809 OMIM:144250
J:37861




Genotype
MGI:4941579
cx2
Allelic
Composition
Ldlrtm1Her/Ldlrtm1Her
Tg(APOC3)3707Bres/?
Tg(Mt1-CETP)#Tall/?
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ldlrtm1Her mutation (19 available); any Ldlr mutation (76 available)
Tg(APOC3)3707Bres mutation (1 available)
Tg(Mt1-CETP)#Tall mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• lowered by 79% on a normal diet
• lowered by 36% on a Western diet
• cholesterol shifted from HDL to IDL-LDL and VLDL
• cholesterol shifted from HDL to IDL-LDL and VLDL
• cholesterol shifted from HDL to IDL-LDL and VLDL
• triglycerides shifted from VLDL to IDL-LDL and HDL




Genotype
MGI:3710973
tg3
Allelic
Composition
Tg(APOC3)3707Bres/0
Genetic
Background
involves: C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(APOC3)3707Bres mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• the mean fasting plasma glucose concentration is essentially identical in transgenic mice and littermate controls
• the mean fasting plasma insulin concentration is essentially identical in transgenic mice and littermate controls
• insulin-mediated glucose uptake does not differ between transgenic mice and littermate controls, based on their attaining similar steady-state plasma glucose (SSPG) and steady-state plasma insulin (SSPI) levels following co-infusion of glucose (14.5 mg/min per g body weight) and insulin (0.2 ng/min per gram body weight)
• the mean fasting cholesterol is significantly higher in 7-8-month old transgenic mice (3.5 +/- 0.2 mmol/l) than in littermate controls (2.4 +/- mmol/l) (P<0.001)
• the mean fasting plasma triglyceride concentration is considerably higher in 7-8-month old transgenic mice (11.8 +/- 0.2 mmol/l) than in littermate controls (1.1 +/- 0.1 mmol/l) (P<0.001)

adipose tissue
N
• epididymal fat pad adipocytes isolated from transgenic and control mice exhibit similar glucose transport rates at a maximal insulin concentration (Vmax)
• the insulin concentration inducing half-maximal glucose transport rate (ED50) is similar in epididymal fat pad adipocytes isolated from transgenic and control mice
• isoproterenol-induced lipolysis, measured by glycerol release, is essentially identical in transgenic and control epididymal fat pad adipocytes over a dose range of 10-9-10-6
• insulin inhibition of isoproterenol-induced lipolysis, as measured by glycerol release, is essentially identical in transgenic and control epididymal fat pad adipocytes





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