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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Agertm1.1Arnd
targeted mutation 1.1, Bernd Arnold
MGI:2451038
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Agertm1.1Arnd/Agertm1.1Arnd B6.129P2-Agertm1.1Arnd MGI:3694553
hm2
Agertm1.1Arnd/Agertm1.1Arnd involves: 129P2/OlaHsd MGI:3696556
hm3
Agertm1.1Arnd/Agertm1.1Arnd involves: 129P2/OlaHsd * C57BL/6 MGI:3694549


Genotype
MGI:3694553
hm1
Allelic
Composition
Agertm1.1Arnd/Agertm1.1Arnd
Genetic
Background
B6.129P2-Agertm1.1Arnd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agertm1.1Arnd mutation (0 available); any Ager mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• mutants have decreased numbers of osteoclasts per bone surface compared to wild-type
• males have increased cortical thickness at 3 months compared to wild-type males
• at 1 and 3 months of age, males have significantly increased bone mineral content (BMC) compared to male wild-type, as seen in femora of males
• at 1 and 3 months of age, males have significantly increased bone mineral density (BMD) compared to male wild-type, as seen in femora of males
• markedly higher trabecular bone volume in the proximal femur at 3 months
• decreased trabecular spacing
• male mutants have increased trabecular thickness
• increased bone mass is observed in males and females starting at 4 weeks of age
• bone resorption is defective in ovariectomized (OVX) mutants; OVX mutants are resistant to bone loss unlike OVX wild-type mice
• biomechanical bone strength and flexibility is increased in 3-month old mice compared to wild-type

limbs/digits/tail
• males have increased cortical thickness at 3 months compared to wild-type males

homeostasis/metabolism
• mutants exhibit significantly lower serum IL-6 levels at 3 months of age, but not 1 month, compared to wild-type

immune system
• mutants have decreased numbers of osteoclasts per bone surface compared to wild-type
• mutants exhibit significantly lower serum IL-6 levels at 3 months of age, but not 1 month, compared to wild-type

hematopoietic system
• mutants have decreased numbers of osteoclasts per bone surface compared to wild-type




Genotype
MGI:3696556
hm2
Allelic
Composition
Agertm1.1Arnd/Agertm1.1Arnd
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agertm1.1Arnd mutation (0 available); any Ager mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• application of carboxymethyllysine-modified proteins (CML-mps) to rectosigmoid colon of mice does not activate NF kappa B in mutants or induce tissue inflammation whereas both are observed in treated wild-type mice

cellular
• mouse embryonic fibroblasts (MEFs) exhibit impaired chemotaxis in response to HMGB1 compared with wild-type cells
• however, chemotaxis in response to PDGF is normal




Genotype
MGI:3694549
hm3
Allelic
Composition
Agertm1.1Arnd/Agertm1.1Arnd
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agertm1.1Arnd mutation (0 available); any Ager mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mice show markedly decreased neointimal expansion after femoral artery denudation injury
• after streptozocin treatment, mutants and controls display serum glucose >250 mg/dl; >95% of mice develop diabetes
• after 12 weeks of disease, blood glucose in mutants measures 441 mg/dl, not significantly different from 473 mg/dl in diabetic controls

renal/urinary system
• after 12 weeks of diabetes in mutants, glomerular basement membrane thickness is increased ~3% compared to non-diabetic mutant controls while diabetic wild-type controls show ~14% increased thickness compared to non-diabetic wild-type controls
• after 12 weeks, diabetic mutants display a ~5% increase in glomerular area compared to non-diabetic mutant controls, while diabetic wild-type controls exhibit an increase of ~18% in glomerular area
• after 12 weeks, diabetic mutants display a 6% decrease in mesangial area compared to non-diabetic mutant controls, while diabetic wild-type controls exhibit an increases of ~61%
• diabetic mutant mice show no increase in kidney weight/body weight ratio after 12 weeks of disease whereas diabetic wild-type controls show a 1.6 fold increase in this parameter

cardiovascular system
• VSM cell migration induced by calgranulin b is markedly decreased
• VSM cell proliferation induced by calgranulin b is blunted
• mice show markedly decreased neointimal expansion after femoral artery denudation injury

muscle
• VSM cell migration induced by calgranulin b is markedly decreased
• VSM cell proliferation induced by calgranulin b is blunted

behavior/neurological
• homozygous mice are partially protected from the increased nociceptive threshold caused by diabetes

cellular
• VSM cell proliferation induced by calgranulin b is blunted





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory