- decreased circulating chloride level / IMPC
- abnormal kidney morphology / IMPC
- abnormal urinary bladder morphology / IMPC
- abnormal spleen morphology / IMPC
- small testis / IMPC
- abnormal heart morphology / IMPC
- decreased thigmotaxis / IMPC
- decreased body weight / IMPC
- increased lung elastance / IMPC
- increased blood urea nitrogen level / IMPC
- abnormal testis morphology / IMPC
- abnormal skin morphology / IMPC
- enlarged heart / IMPC
- decreased mean platelet volume / IMPC
- increased fasting circulating glucose level / IMPC
C57BL/6N-Atm1Brd Atf2tm1a(EUCOMM)Hmgu/Ph
Status | Available to order |
EMMA ID | EM:09148 |
International strain name | C57BL/6N-Atm1Brd Atf2tm1a(EUCOMM)Hmgu/Ph |
Alternative name | B6.Atf2tm1a |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Atf2tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Atf2 |
Information from provider
Provider | Regine Schneider-Stock |
Provider affiliation | Pathologisches Institut , Universitätsklinikum Erlangen |
Genetic information | Atf2 gene was conditionally targeted by insertion of a reporter-tagged cassette containing lacZ, neomycin resistance, Frt and LoxP sequences. Exons 6-7 were targeted by homologous recombination and electroporation of the targeting construct into C57BL/6N-A/a ES cells. The targeting resulted in a so called "knockout-first allele". LacZ and neomycin cassettes together are flanked by Frt sites; neomycin cassette and targeted exons 6-7 are flanked by LoxP sites. Positive targeted ES cell clones were injected into C57BL/6N embryos. |
Phenotypic information | Homozygous:The strain was not bred for homozygous mice. Phenotype unknown.Heterozygous:Heterozygous mice appear normal like wild-type animals. No obvious phenotype. |
Breeding history | Chimeric mice were paired with wild-type C57BL/6N partners to test for germ-line transmission and to obtain heterozygous F1 generation mice. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Animals used for archiving | heterozygous C57BL/6NCrl |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal chondrocyte morphology / MGI
- short limbs / MGI
- tremors / MGI
- decreased brain size / MGI
- decreased Purkinje cell number / MGI
- ectopic Purkinje cell / MGI
- abnormal lung morphology / MGI
- decreased body weight / MGI
- increased metastatic potential / MGI
- ataxia / MGI
- hyperactivity / MGI
- impaired limb coordination / MGI
- cyanosis / MGI
- abnormal placenta labyrinth morphology / MGI
- eye inflammation / MGI
- respiratory failure / MGI
- postnatal lethality / MGI
- no abnormal phenotype detected / MGI
- increased susceptibility to bacterial infection / MGI
- increased susceptibility to viral infection / MGI
- chondrodystrophy / MGI
- head shaking / MGI
- abnormal vestibular ganglion morphology / MGI
- abnormal cytokine secretion / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- decreased otolith number / MGI
- abnormal placenta vasculature / MGI
- abnormal artery development / MGI
- decreased vestibular hair cell number / MGI
- abnormal vestibular saccular macula morphology / MGI
- abnormal utricular macula morphology / MGI
- decreased vestibular hair cell stereocilia number / MGI
- hypoxia / MGI
- head tossing / MGI
- immune system phenotype / MGI
- impaired hearing / MGI
- decreased long bone epiphyseal plate size / MGI
- disorganized long bone epiphyseal plate / MGI
- decreased NK T cell number / MGI
- decreased NK cell number / MGI
- decreased circulating interferon-gamma level / MGI
- increased susceptibility to endotoxin shock / MGI
- proportional dwarf / MGI
- abnormal NK cell physiology / MGI
- lethality at weaning, complete penetrance / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- enlarged brain ventricles / MGI
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