- increased monocyte cell number / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- increased neutrophil cell number / IMPC
- increased lymphocyte cell number / IMPC
- abnormal gait / IMPC
- impaired righting response / IMPC
- decreased mean corpuscular volume / IMPC
- enlarged lymph nodes / IMPC
- decreased lymphocyte cell number / IMPC
- decreased bone mineral content / IMPC
- increased leukocyte cell number / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- increased large unstained cell number / IMPC
- increased eosinophil cell number / IMPC
- increased basophil cell number / IMPC
CD1.Cg-Stat1tm1Dlv/Cnbc
Status | Available to order |
EMMA ID | EM:06065 |
International strain name | CD1.Cg-Stat1tm1Dlv/Cnbc |
Alternative name | CD1.129-Stat1 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Stat1tm1Dlv |
Gene/Transgene symbol | Stat1 |
Information from provider
Provider | Luis Enjuanes |
Provider affiliation | Centro Nacional de Biotecnologia (CNB-CSIC) |
Additional owner | There are 14 strains of Stat1 KO available through IMSR, including the one used here from David Levy's lab at NYU (Stat1 |
Genetic information | Transgenic mice were produced in ICR (CD1) mouse outbred background by standard pronuclear microinjection and bred to homozygosity. Stat1 KO mice were produced and donated by David Levy (NYU) in 129S/Sv (CCE ES cells) background and backcrossed to CD1 mouse background to homozygosity. A neomycin resistance cassette replaced 5.7 kb of sequence, including 3 exons and a portion of a fourth encoding amino acids 221-365. This allele produces a partial non-functional protein product. Both mouse lines were bred to double homozygosity in CD1 background. Line 270 and 861 expressed the highest levels of APN. These mice are double homozygous for non-transgenic line APN (wild-type) and double homozygous for Stat1 KO mutation. |
Phenotypic information | Immunocompromised (due to Stat1 deficit) mice, control mice for the entire experiment. |
Breeding history | Stat1 KO mice originally generated in 129S/Sv background (CCE ES cells) and backcrossed to CD1. Tg APN mice generated in CD1(ICR) mice. Both mouse lines bred to double homozygous line. In this case Stat1 locus carries both KO alleles and no APN transgene is included |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | yes |
Immunocompromised | yes |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome / Orphanet_391487
- Susceptibility to viral and mycobacterial infections due to STAT1 deficiency / Orphanet_391311
- Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency / Orphanet_319595
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- increased mammary adenocarcinoma incidence / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- increased circulating interferon-gamma level / MGI
- increased circulating interleukin-12b level / MGI
- abnormal NK cell physiology / MGI
- decreased level of surface class I molecules / MGI
- increased susceptibility to bacterial infection / MGI
- increased susceptibility to viral infection / MGI
- abnormal MHC II cell surface expression on macrophages / MGI
- vision/eye phenotype / MGI
- decreased susceptibility to endotoxin shock / MGI
- abnormal intestine morphology / MGI
- decreased body size / MGI
- multifocal hepatic necrosis / MGI
- abnormal leukocyte physiology / MGI
- lethality at weaning, complete penetrance / MGI
MGI phenotypes (gene matching)
- abnormal intestine morphology / MGI
- abnormal tibia morphology / MGI
- decreased body size / MGI
- abnormal cornea morphology / MGI
- multifocal hepatic necrosis / MGI
- abnormal T cell activation / MGI
- decreased level of surface class I molecules / MGI
- increased mammary adenocarcinoma incidence / MGI
- no abnormal phenotype detected / MGI
- increased susceptibility to bacterial infection / MGI
- increased susceptibility to viral infection / MGI
- abnormal leukocyte physiology / MGI
- abnormal macrophage physiology / MGI
- increased IgG level / MGI
- increased myocardial infarction size / MGI
- abnormal cell cycle / MGI
- abnormal redox activity / MGI
- increased cardiomyocyte apoptosis / MGI
- abnormal nitric oxide homeostasis / MGI
- increased compact bone thickness / MGI
- decreased B-1 B cell number / MGI
- increased osteoclast cell number / MGI
- increased bone resorption / MGI
- decreased B cell number / MGI
- abnormal response to infection / MGI
- abnormal MHC II cell surface expression on macrophages / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- immune system phenotype / MGI
- vision/eye phenotype / MGI
- abnormal T-helper 2 physiology / MGI
- increased bone mass / MGI
- abnormal cell physiology / MGI
- abnormal common myeloid progenitor cell morphology / MGI
- increased NK T cell number / MGI
- decreased NK cell number / MGI
- increased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- decreased single-positive T cell number / MGI
- decreased susceptibility to neuronal excitotoxicity / MGI
- abnormal osteoblast differentiation / MGI
- abnormal osteoclast differentiation / MGI
- decreased interferon-gamma secretion / MGI
- increased circulating interferon-gamma level / MGI
- decreased circulating interferon-gamma level / MGI
- increased circulating interleukin-12b level / MGI
- decreased interleukin-1 beta secretion / MGI
- decreased susceptibility to endotoxin shock / MGI
- decreased NK cell degranulation / MGI
- decreased hepatocyte apoptosis / MGI
- decreased sensitivity to induced cell death / MGI
- increased susceptibility to bacterial infection induced morbidity/mortality / MGI
- tumor regression / MGI
- abnormal NK cell physiology / MGI
- increased effector memory CD8-positive, alpha-beta T cell number / MGI
- increased trabecular bone volume / MGI
- increased compact bone volume / MGI
- increased macrophage nitric oxide production / MGI
- lethality at weaning, complete penetrance / MGI
- abnormal CD8-positive, naive alpha-beta T cell number / MGI
Literature references
- Development of a transgenic mouse model susceptible to human coronavirus 229E.;Lassnig Caroline, Sanchez Carlos M, Egerbacher Monika, Walter Ingrid, Majer Susanne, Kolbe Thomas, Pallares Pilar, Enjuanes Luis, Müller Mathias, ;2005;Proceedings of the National Academy of Sciences of the United States of America;102;8275-80; 15919828
- Targeted disruption of the mouse Stat1 gene results in compromised innate immunity to viral disease.;Durbin J E, Hackenmiller R, Simon M C, Levy D E, ;1996;Cell;84;443-50; 8608598
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