About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Atf2tm1Glm
targeted mutation 1, Laurie Glimcher
MGI:1857283
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Atf2tm1Glm/Atf2tm1Glm C.Cg-Atf2tm1Glm MGI:3046403
hm2
Atf2tm1Glm/Atf2tm1Glm involves: 129S2/SvPas MGI:2655609
ht3
Atf2tm1Glm/Atf2+ involves: 129S2/SvPas MGI:3046342
ht4
Atf2tm1Glm/Atf2tm1Sis involves: 129S2/SvPas * C57BL/6 * CBA MGI:3842393


Genotype
MGI:3046403
hm1
Allelic
Composition
Atf2tm1Glm/Atf2tm1Glm
Genetic
Background
C.Cg-Atf2tm1Glm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atf2tm1Glm mutation (1 available); any Atf2 mutation (89 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• homozygotes display a slight reduction in body mass

immune system
N
• homozygotes show normal counts of circulating granulocytes and normal lymphocyte cell numbers in lymph nodes, spleen and thymus
• three hours after T cell activation via i.v. injection with anti-CD3 antibody, mutant spleens display less induction of IL-2, IL-4 and IL-6 mRNA compared with wild-type spleens
• notably, T lymphocytes from anti-CD3-treated mutant mice produce normal levels of IL-2 at 24 hours and of IFN-gamma, IL-4, and IL-6 at 48 hours
• homozygotes display increased susceptibility to death from LPS plus D-galactosamine injection
• within 3 hours of challenge by LPS, homozygotes display decreased induction of the adhesion molecules E-selectin, P-selectin and VCAM1, as well as the cytokines tumor necrosis factor, interleukin 1 beta (IL1B) and IL-6, and CXCL1 compared with wild-type
• following exposure to Herpes simplex virus-1, homozygotes exhibit a higher incidence of mononuclear pulmonary infiltrates than wild-type control mice
• homozygotes are more susceptible to Coxsackievirus B3 infection than wild-type control mice




Genotype
MGI:2655609
hm2
Allelic
Composition
Atf2tm1Glm/Atf2tm1Glm
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atf2tm1Glm mutation (1 available); any Atf2 mutation (89 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 51% of homozygous null mice survive past 1 month
• two waves of deaths occur: one within the initial 2 days of life and one near weaning
• the lifespan of surviving homozygotes is, however, normal

behavior/neurological
• homozygotes show a characteristic fine-amplitude whole-body tremor
• homozygotes exhibit decreased hind limb coordination
• homozygotes display abnormal twitches of the head
• homozygotes exhibit vertical head tossing

growth/size/body
• surviving homozygotes reach approximately 71% of the weight of sex-matched wild-type littermates
• surviving homozygotes are mildly to severely runted
• dwarfism is uniform, with the reduced spine length proportional to the shortened extremities

hearing/vestibular/ear
• significant reductions in numbers of vestibular sensory cells
• significant reductions in numbers of vestibular hair cell stereocilia
• the macula of utricle is atrophic, with significant reductions in numbers of sensory cells, stereocilia and otoconia
• the macula of the saccule is atrophic, with significant reductions in numbers of sensory cells, stereocilia and otoconia
• significant reductions in numbers of otoconia
• homozygotes display decreased hearing

immune system
• 50% of homozygotes spontaneously develop periocular neutrophilic/lymphocytic infiltrates
• in contrast to wild-type, homozygotes display poor induction of E-selectin three hours after intraperitoneal injection of LPS at doses up to 50 microg
• higher doses of LPS lead to equal induction of E-selectin mRNA in both genotypes

limbs/digits/tail
• the limb length decrease is rhizomelic, with more severe shortening in proximal bony segments than distal ones

skeleton
• in vivo labelling of cartilage cells with 3H-thymidine confirmed that growth-plate cartilage cell division is significantly reduced
• homozygotes lack normal-appearing cartilaginous trabeculae extending from the physes and have distinctly thin epiphyseal growth plates
• bones show disorganization in the sequence of endochondral ossification at epiphyseal growth plates
• homozygotes exhibit abnormal clusters of cells instead of ordered columns of chondrocytes, seams of bone covering the metaphyseal side of the physes, and lack of ingrowth of chondroclasts and capillaries
• the dysmorphology of epiphyseal plates coupled with the variable penetrance of the bone abnormality is reminiscent of human hypochondroplasia

nervous system
• significant reductions in numbers of vestibular sensory cells
• significant reductions in numbers of vestibular hair cell stereocilia
• brains of homozygous null mice display enlarged ventricles
• homozygotes display a 50% decrease in Purkinje cells at the cerebellar molecular-granular cell layer boundary
• numerous large Purkinje-like cells are distributed throughtout the otherwise normal-appearing granular cell layer of the cerebellum
• vestibular ganglia have decreased neuron cell bodies

vision/eye
• 50% of homozygotes spontaneously develop periocular neutrophilic/lymphocytic infiltrates

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
osteochondrodysplasia DOID:2256 J:30611




Genotype
MGI:3046342
ht3
Allelic
Composition
Atf2tm1Glm/Atf2+
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atf2tm1Glm mutation (1 available); any Atf2 mutation (89 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• heterozygous mice are phenotypically normal but display an increased postnatal mortality rate that is roughly half that of homozygotes, consistent with a gene dosage effect




Genotype
MGI:3842393
ht4
Allelic
Composition
Atf2tm1Glm/Atf2tm1Sis
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atf2tm1Glm mutation (1 available); any Atf2 mutation (89 available)
Atf2tm1Sis mutation (2 available); any Atf2 mutation (89 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

respiratory system





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
04/23/2024
MGI 6.23
The Jackson Laboratory