- increased monocyte cell number / MGI
- sparse hair / MGI
- lymphoid hyperplasia / MGI
- skin hyperplasia / MGI
- hyperkeratosis / MGI
- disheveled coat / MGI
- skin edema / MGI
- abnormal inflammatory response / MGI
- abnormal skin morphology / MGI
- abnormal macrophage physiology / MGI
- increased IgA level / MGI
- decreased basophil cell number / MGI
- abnormal cytokine secretion / MGI
- no phenotypic analysis / MGI
- liver degeneration / MGI
- pallor / MGI
- liver hemorrhage / MGI
- skin inflammation / MGI
- increased spleen weight / MGI
- dermal hyperplasia / MGI
- decreased eosinophil cell number / MGI
- increased NK T cell number / MGI
- decreased NK T cell number / MGI
- increased circulating tumor necrosis factor level / MGI
- abnormal interferon secretion / MGI
- increased tumor necrosis factor secretion / MGI
- decreased interferon-beta secretion / MGI
- increased circulating interleukin-10 level / MGI
- increased circulating interleukin-6 level / MGI
- increased circulating interleukin-1 beta level / MGI
- increased interleukin-6 secretion / MGI
- abnormal cytokine level / MGI
- increased susceptibility to endotoxin shock / MGI
- abnormal hair cycle anagen phase / MGI
- increased susceptibility to bacterial infection induced morbidity/mortality / MGI
- postnatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
C57BL/6NCrl-Tbk1em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:12874 |
Citation information | RRID:IMSR_EM:12874 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-Tbk1em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Tbk1em1(IMPC)Ccpcz |
Gene/Transgene symbol | Tbk1 |
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
- Frontotemporal dementia with motor neuron disease / Orphanet_275872
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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