- increased susceptibility to bacterial infection / MGI
- abnormal macrophage physiology / MGI
- abnormal cytokine secretion / MGI
- decreased acute inflammation / MGI
- decreased B cell proliferation / MGI
- immune system phenotype / MGI
- abnormal cell physiology / MGI
- decreased circulating tumor necrosis factor level / MGI
- decreased tumor necrosis factor secretion / MGI
- decreased interferon-alpha secretion / MGI
- decreased interferon-beta secretion / MGI
- decreased circulating interferon-gamma level / MGI
- decreased circulating interleukin-1 level / MGI
- decreased circulating interleukin-6 level / MGI
- decreased interleukin-12b secretion / MGI
- decreased interleukin-6 secretion / MGI
- abnormal cytokine level / MGI
- abnormal chemokine secretion / MGI
- decreased susceptibility to endotoxin shock / MGI
- abnormal NK cell physiology / MGI
C57BL/6NCrl-Irak4em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:12792 |
Citation information | RRID:IMSR_EM:12792 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6NCrl-Irak4em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Irak4em1(IMPC)Ccpcz |
Gene/Transgene symbol | Irak4 |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency / Orphanet_70592
MGI phenotypes (gene matching)
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