About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cnot3tm1.1Tya
targeted mutation 1.1, Tadashi Yamamoto
MGI:5607530
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cnot3tm1.1Tya/Cnot3tm1.1Tya B6.129P2(Cg)-Cnot3tm1.1Tya MGI:5607533
ht2
Cnot3tm1.1Tya/Cnot3+ B6.129P2(Cg)-Cnot3tm1.1Tya MGI:5607531
cx3
Cnot3tm1.1Tya/Cnot3+
Lepob/Lepob
involves: 129P2/OlaHsd * C57BL/6J MGI:5607532


Genotype
MGI:5607533
hm1
Allelic
Composition
Cnot3tm1.1Tya/Cnot3tm1.1Tya
Genetic
Background
B6.129P2(Cg)-Cnot3tm1.1Tya
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnot3tm1.1Tya mutation (0 available); any Cnot3 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:5607531
ht2
Allelic
Composition
Cnot3tm1.1Tya/Cnot3+
Genetic
Background
B6.129P2(Cg)-Cnot3tm1.1Tya
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnot3tm1.1Tya mutation (0 available); any Cnot3 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• mice fed a high-fat diet for 12 weeks show that subcutaneous fat depots are greatly decreased in mutants
• mice fed a high-fat diet for 12 weeks show that visceral fat depots are greatly decreased in mutants
• weights of adipose tissues are decreased

growth/size/body
• mice fed a high-fat diet for 12 weeks show that visceral fat depots are greatly decreased in mutants
• smaller body size that is apparent in newborns and remains throughout development
• at 12 weeks of age, mice weight about 20% less than wild-type mice
• the nose-anus length is reduced by about 5% at 12 weeks of age
• mice fed a high-fat diet for 12 weeks become less obese than wild-type mice, with weight of liver, white adipose tissue and brown adipose tissue less than that of wild-type mice on the same diet

homeostasis/metabolism
• mice fed a high-fat diet for 12 weeks become less obese than wild-type mice, with weight of liver, white adipose tissue and brown adipose tissue less than that of wild-type mice on the same diet
• mice fed a high-fat diet for 12 weeks exhibit lower blood glucose levels and remain lower in both glucose tolerance and insulin tolerance tests
• decrease in blood glucose under fasting conditions
• however, no differences in serum insulin levels
• decrease in serum triglyceride levels under feeding and fasting conditions
• whole-body oxygen consumption is higher during dark and light periods, with 24 hour oxygen consumption rates 20% higher than in wild-type mice
• however, rectal temperature is normal
• glucose tolerance test shows that blood glucose levels remain lower than in wild-type mice after glucose administration
• mice fed a high-fat diet for 12 weeks remain lower in the glucose tolerance test
• however, the insulin response was similar to wild-type mice
• insulin tolerance test shows a greater decrease in blood glucose levels in mutants than in wild-type mice in response to insulin
• mice are insulin sensitive even on a high-fat diet

integument
• mice fed a high-fat diet for 12 weeks show that subcutaneous fat depots are greatly decreased in mutants

liver/biliary system
• mice fed a high-fat diet for 12 weeks show less fatty liver development than wild-type mice

cellular
• RANKL-induced osteoclastogenesis in bone marrow cells is enhanced, indicating an increase in differentiation into osteoclasts

hematopoietic system
• RANKL-induced osteoclastogenesis in bone marrow cells is enhanced, indicating an increase in differentiation into osteoclasts
• increase in the number of osteoclasts per bone surface and in the levels of osteoclast surface per bone surface

immune system
• RANKL-induced osteoclastogenesis in bone marrow cells is enhanced, indicating an increase in differentiation into osteoclasts
• increase in the number of osteoclasts per bone surface and in the levels of osteoclast surface per bone surface

skeleton
• increase in the number of osteoclasts per bone surface and in the levels of osteoclast surface per bone surface
• decrease in bone mineral density at 4 months of age
• aged mice (2 years) show a decrease in cortical bone thickness
• trabecular bone exhibits a sparse osteoporotic pattern at 4 months of age
• increase in the levels of trabecular separation and trabecular spacing at 4 months of age, which increases with age
• decrease in trabecular number at 4 months of age
• aging induced osteoporosis results in a 3-fold reduction in the baseline levels of trabecular number compared to 4 month old mutants
• decrease in trabecular bone mass at 4 months of age
• trabecular thickness is slightly reduced but is not significant, however aged mice show reduced thickness of trabecular bone
• decrease in levels of the bone volume per tissue volume at 4 months of age
• osteoporosis is exacerbated with age, with bone volume further reduced by about 50% at 2 years of age, and a further increase in trabecular separation and trabecular spacing and bone resorption
• elevation in levels of bone formation rate
• RANKL-induced osteoclastogenesis in bone marrow cells is enhanced, indicating an increase in differentiation into osteoclasts
• mice show an increase in mineralizing surface per bone surface which represents the number of active osteoblasts per bone surface
• increase in the number of osteoclasts per bone surface and in the levels of osteoclast surface per bone surface indicating that bone resorption is increased




Genotype
MGI:5607532
cx3
Allelic
Composition
Cnot3tm1.1Tya/Cnot3+
Lepob/Lepob
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cnot3tm1.1Tya mutation (0 available); any Cnot3 mutation (35 available)
Lepob mutation (5 available); any Lep mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mice are less obese than single homozygous Lepob mice

homeostasis/metabolism
• oxygen consumption rate is increased and respiratory quotient is lower compared to single homozygous Lepob> mice, indicating greater utilization of fat versus carbohydrates as energy source
• oxygen consumption rate is increased and respiratory quotient is lower compared to single homozygous Lepob> mice, indicating greater utilization of fat versus carbohydrates as energy source
• glucose tolerance is ameliorated compared to single homozygous Lepob mice
• insulin sensitivity is ameliorated compared to single homozygous Lepob mice

behavior/neurological
N
• no differences in locomotor activity or food intake compared to single homozygous Lepob mice





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory