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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Jundtm1Mya
targeted mutation 1, Moshe Yaniv
MGI:2385829
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Jundtm1Mya/Jundtm1Mya either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6) MGI:3057306
hm2
Jundtm1Mya/Jundtm1Mya involves: 129S2/SvPas * C57BL/6 MGI:3639590
hm3
Jundtm1Mya/Jundtm1Mya involves: 129S2/SvPas * C57BL/6J MGI:5586556
cx4
Juntm6.1(Jund)Wag/Juntm6.1(Jund)Wag
Jundtm1Mya/Jundtm1Mya
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:5284981
cx5
Jundtm1Mya/Jundtm1Mya
Tg(H2-K-Fosl1)1Wag/0
involves: 129S2/SvPas * C57BL/6 * CBA MGI:3639603


Genotype
MGI:3057306
hm1
Allelic
Composition
Jundtm1Mya/Jundtm1Mya
Genetic
Background
either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jundtm1Mya mutation (0 available); any Jund mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• male homozygotes fail to show any mating behavior or vaginal plugs in the presence of wild-type females in estrus, or superovulated females

cellular
• group I of male homozygotes exhibit oligo-astheno-teratospermia
• group I of male homozygotes exhibit oligo-astheno-teratospermia with distinct head and flagellum anomalies, including a hammer-like head shape
• in addition to the proliferative defect, primary MEFs show a 33% increase in the G0/G1 population, and appear enlarged and flat indicating premature senescence
• mutant MEFs exhibit a Trp53-dependent hypersensitivity (2.5- to 5-fold) to UV-induced cell death; removal of Trp53 overcomes the UV hypersensitivity
• group II of male homozygotes contain sperm of normal morphology and concentration but display a significantly impaired sperm motility
• group I of male homozygotes exhibit oligo-astheno-teratospermia
• primary MEFs exhibit a significant reduction in cell colony growth upon plating at low density
• in contrast to primary cells, immortalized fibroblast cell lines show increased proliferation associated with higher cyclin D1 levels
• also, immortalized fibroblast cell lines have spindle-like morphology and tend to pile up at high cell densities
• T cells from homozygous mutant mice hyperproliferate following mitogen induction with anti-CD3 plus anti-CD28 or with PMA plus ionomycin
• in contrast, the proliferation of mutant T cells in response to concanavalin A remains unaffected

endocrine/exocrine glands
• group I of sterile males shows a complete absence of flagella in the lumen of the seminiferous tubules
• in stage VII tubules, complete loss of flagella correlates with a significant reduction in the number of late spermatid heads

growth/size/body
• homozygotes are viable and healthy but exhibit a postnatal growth retardation relative to wild-type
• however, no gross abnormalities are observed in the kidney, brain, stomach, gut, heart, skin, or pituitary up to 18 months

homeostasis/metabolism
• mutant males display a significant increase in inhibin B levels and a corresponding decrease in FSH levels
• homozygotes display a 30% reduction in total pituitary GH levels
• homozygotes display a 30% reduction in circulating GH levels in serum

immune system
N
• homozygotes show no major changes in hematopoietic lineages or signs of severe infection
• T cells from homozygous mutant mice hyperproliferate following mitogen induction with anti-CD3 plus anti-CD28 or with PMA plus ionomycin
• in contrast, the proliferation of mutant T cells in response to concanavalin A remains unaffected
• mutant Th2 cells secrete higher amounts of both IL-4 and IL-10 relative to wild-type Th2 cells
• mutant Th2 cells also produce high levels of the Th1-specific cytokine IFN-gamma, which is also increased in polarized Th1 cells CD4+ T cells
• following LPS/galactosamine treatment, homozygotes exhibit earlier lethality than wild-type; only 36% of homozygotes survive compared to 82% of wild-type
• homozygotes are significantly sensitive to LPS-induced hepatitis, with nearly all hepatocyte nuclei showing signs of apoptosis; in contrast, little hepatocyte apoptosis is noted in wild-type

reproductive system
N
• female homozygotes show no severe reproductive defects and produce litters of normal size
• male homozygotes show no differences in testosterone levels or in the weight of seminal vesicles relative to wild-type
• group II of male homozygotes contain sperm of normal morphology and concentration but display a significantly impaired sperm motility
• group I of male homozygotes exhibit oligo-astheno-teratospermia
• group I of sterile males shows a complete absence of flagella in the lumen of the seminiferous tubules
• in stage VII tubules, complete loss of flagella correlates with a significant reduction in the number of late spermatid heads
• homozygotes exhibit heterogeneous spermatogenic defects (group I and II)
• however, testicular weight is normal
• group I of male homozygotes exhibit oligo-astheno-teratospermia
• group I of male homozygotes exhibit oligo-astheno-teratospermia with distinct head and flagellum anomalies, including a hammer-like head shape
• 25% of male homozygotes fail to produce any litters over a 2-month breeding period
• the remaining males display an age-dependent drop in fertility and cease to produce litters as they grow older

liver/biliary system
• homozygotes are significantly sensitive to LPS-induced hepatitis, with nearly all hepatocyte nuclei showing signs of apoptosis; in contrast, little hepatocyte apoptosis is noted in wild-type

hematopoietic system
• T cells from homozygous mutant mice hyperproliferate following mitogen induction with anti-CD3 plus anti-CD28 or with PMA plus ionomycin
• in contrast, the proliferation of mutant T cells in response to concanavalin A remains unaffected
• mutant Th2 cells secrete higher amounts of both IL-4 and IL-10 relative to wild-type Th2 cells
• mutant Th2 cells also produce high levels of the Th1-specific cytokine IFN-gamma, which is also increased in polarized Th1 cells CD4+ T cells




Genotype
MGI:3639590
hm2
Allelic
Composition
Jundtm1Mya/Jundtm1Mya
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jundtm1Mya mutation (0 available); any Jund mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• develop less adaptive myocardial hypertrophy in response to chronic pressure overload than controls

homeostasis/metabolism
• develop less adaptive myocardial hypertrophy in response to chronic pressure overload than controls




Genotype
MGI:5586556
hm3
Allelic
Composition
Jundtm1Mya/Jundtm1Mya
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jundtm1Mya mutation (0 available); any Jund mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
• in mice fed a high fat diet
• in mice fed a high fat diet
• however, relative liver weight is normal in mice fed a high fat diet
• mice fed a high fat diet exhibit reduced steatohepatitis compared with control mice

homeostasis/metabolism
• whether fed normal chow or a high fat diet
• in fasted mice fed normal chow
• in mice fed a high fat diet

growth/size/body
• whether fed normal chow or a high fat diet

adipose tissue
• in mice fed a high fat diet




Genotype
MGI:5284981
cx4
Allelic
Composition
Juntm6.1(Jund)Wag/Juntm6.1(Jund)Wag
Jundtm1Mya/Jundtm1Mya
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jundtm1Mya mutation (0 available); any Jund mutation (3 available)
Juntm6.1(Jund)Wag mutation (0 available); any Jun mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cellular
• in mouse embryonic fibroblasts
• in mouse embryonic fibroblasts

embryo

growth/size/body




Genotype
MGI:3639603
cx5
Allelic
Composition
Jundtm1Mya/Jundtm1Mya
Tg(H2-K-Fosl1)1Wag/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jundtm1Mya mutation (0 available); any Jund mutation (3 available)
Tg(H2-K-Fosl1)1Wag mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 60% die within the first 2 weeks after birth

cardiovascular system
• show signs of advanced chronic hepatic and pulmonary congestion
• mitochondria are randomly dispersed in clusters and appear swollen
• cardiomyocyte hypertrophy and disarray
• extensive focal interstitial fibrosis in ventricles
• heart size of adults is increased

cellular
• extensive focal interstitial fibrosis in ventricles
• MEFs exhibit a marked increase in basal polarization of mitochondria and fast mitochondrial depolarization in response to oligomycin

homeostasis/metabolism
• mutants surviving the first month after birth develop peripheral edema
• mutants surviving the first month after birth develop ascites

behavior/neurological
• mutants surviving the first month after birth become lethargic

muscle
• mitochondria are randomly dispersed in clusters and appear swollen
• heart size of adults is increased

respiratory system
• mutants surviving the first month after birth become dyspneic

liver/biliary system

growth/size/body
• cardiomyocyte hypertrophy and disarray

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
dilated cardiomyopathy DOID:12930 OMIM:PS115200
J:95691





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory