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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mark3tm1Hpw
targeted mutation 1, Helen Piwnica-Worms
MGI:3836595
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mark3tm1Hpw/Mark3tm1Hpw involves: 129X1/SvJ * C57BL/6 MGI:4830568
cx2
Mark2tm1Hpw/Mark2tm1Hpw
Mark3tm1Hpw/Mark3tm1Hpw
involves: 129X1/SvJ * C57BL/6 MGI:4830569
cx3
Mark2tm1Hpw/Mark2+
Mark3tm1Hpw/Mark3tm1Hpw
involves: 129X1/SvJ * C57BL/6 MGI:4830570
cx4
Mark2tm1Hpw/Mark2tm1Hpw
Mark3tm1Hpw/Mark3+
involves: 129X1/SvJ * C57BL/6 MGI:4830571


Genotype
MGI:4830568
hm1
Allelic
Composition
Mark3tm1Hpw/Mark3tm1Hpw
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mark3tm1Hpw mutation (1 available); any Mark3 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• on a regular diet, mice exhibit a decrease in white adipose tissue (WAT) glucose uptake, however on a high-fat diet, uptake is increased so that the difference of glucose uptake in comparison to wild-type on a high-fat diet is eliminated

mortality/aging
• only 17% of the expected 25% of pups were observed

adipose tissue
• brown adipose tissue is disproportionally smaller in mice on a regular diet
• white adipose tissue from gonadal fat pads is disproportionately smaller in mice on a regular diet
• on a regular diet, adiposity is reduced with unaltered glucose handling and normal insulin sensitivity
• however when fed a high-fat diet, mice show a similar increase in overall adiposity as controls
• on a regular diet, mice exhibit a decrease in white adipose tissue (WAT) glucose uptake, however on a high-fat diet, uptake is increased so that the difference of glucose uptake in comparison to wild-type on a high-fat diet is eliminated

growth/size/body
• 9% reduction in body weight at 32 weeks of age when fed a regular diet
• decrease in body weight is observed at 32 weeks of age but not at 6 weeks of age
• mice are protected against high-fat-diet induced obesity, showing weight gain that is delayed and at a reduced rate; mice require 7 additional weeks of high-fat diet to reach the original weight of the wild-type mice

homeostasis/metabolism
• overnight starvation leads to complete hepatic glycogen depletion, associated with hypoketotic hypoglycemia
• mice on a high-fat diet exhibit lower serum insulin levels during the first 60 min of the glucose tolerance test
• however, normal serum insulin levels when fed a regular diet
• males on a regular diet exhibit 10% increase in total energy expenditure
• mice are protected against high-fat-diet induced obesity, showing weight gain that is delayed and at a reduced rate; mice require 7 additional weeks of high-fat diet to reach the original weight of the wild-type mice
• mice exhibit improved glucose tolerance on a high-fat diet compared to wild-type mice on the same diet
• mutants on a high-fat diet are normoglycemic
• normal glucose sensitivity on a regular diet
• decrease in glycogen deposition in the liver
• overnight starvation leads to complete hepatic glycogen depletion compared to partial depletion in wild-type liver and absence of restoration of hepatic glycogen content
• males on a regular diet show a 1.6-fold higher level of serum adiponectin
• males on a regular diet exhibit higher oxygen consumption, with an approximate 9% increase in the total metabolic rate
• however, body temperature, food intake and activity levels are similar to wild-type mice

liver/biliary system
• decrease in glycogen deposition in the liver
• overnight starvation leads to complete hepatic glycogen depletion compared to partial depletion in wild-type liver and absence of restoration of hepatic glycogen content
• mice show resistance to hepatic steatosis after chronic exposure to a high-fat diet, however hepatic glucose uptake is not altered
• overnight starvation results in increased hepatocellular autophagy (increase in autophagic vacuoles in the liver) and increased glycogen synthase levels




Genotype
MGI:4830569
cx2
Allelic
Composition
Mark2tm1Hpw/Mark2tm1Hpw
Mark3tm1Hpw/Mark3tm1Hpw
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mark2tm1Hpw mutation (1 available); any Mark2 mutation (108 available)
Mark3tm1Hpw mutation (1 available); any Mark3 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• complete absence of pups and no mutants are seen at E10.5 or E8.5




Genotype
MGI:4830570
cx3
Allelic
Composition
Mark2tm1Hpw/Mark2+
Mark3tm1Hpw/Mark3tm1Hpw
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mark2tm1Hpw mutation (1 available); any Mark2 mutation (108 available)
Mark3tm1Hpw mutation (1 available); any Mark3 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 2.7% of the expected 12.5% of mutants were recovered and many die shortly after birth

growth/size/body
• 23% reduction in body weight




Genotype
MGI:4830571
cx4
Allelic
Composition
Mark2tm1Hpw/Mark2tm1Hpw
Mark3tm1Hpw/Mark3+
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mark2tm1Hpw mutation (1 available); any Mark2 mutation (108 available)
Mark3tm1Hpw mutation (1 available); any Mark3 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 0.5% of the expected 12.5% of mutants were recovered and many die shortly after birth

growth/size/body
• 30% reduction in body weight





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory