- short tibia / IMPC
B6NCrl;B6N-Atm1Brd Icostm2a(EUCOMM)Wtsi/CipheOrl
Status | Available to order |
EMMA ID | EM:09743 |
Citation information | RRID:IMSR_EM:09743 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 | B6NCrl;B6N-Atm1Brd Icostm2a(EUCOMM)Wtsi/CipheOrl |
Alternative name | EPD0912_4_C07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Icostm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Icos |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Centre d'ImmunoPhenomique - Ciphe |
Provider affiliation | Centre d |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0912_4_C07. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Common variable immunodeficiency / Orphanet_1572
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal leukocyte cell number / MGI
- abnormal small intestine morphology / MGI
- abnormal spleen morphology / MGI
- abnormal immune system physiology / MGI
- decreased IgG level / MGI
- decreased IgA level / MGI
- abnormal T cell differentiation / MGI
- small lymph nodes / MGI
- abnormal spleen germinal center morphology / MGI
- abnormal Peyer's patch germinal center morphology / MGI
- abnormal T cell physiology / MGI
- abnormal B cell number / MGI
- abnormal B cell physiology / MGI
- abnormal immunoglobulin level / MGI
- decreased IgE level / MGI
- decreased anti-insulin autoantibody level / MGI
- abnormal cytokine secretion / MGI
- no phenotypic analysis / MGI
- decreased autoantibody level / MGI
- insulitis / MGI
- increased susceptibility to experimental autoimmune encephalomyelitis / MGI
- decreased susceptibility to autoimmune diabetes / MGI
- abnormal class switch recombination / MGI
- abnormal B cell selection / MGI
- decreased T cell number / MGI
- abnormal response to infection / MGI
- decreased T cell proliferation / MGI
- endocrine/exocrine gland phenotype / MGI
- immune system phenotype / MGI
- abnormal CD4-positive, alpha-beta T cell physiology / MGI
- abnormal T-helper 2 physiology / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- abnormal memory B cell number / MGI
- increased plasma cell number / MGI
- decreased plasma cell number / MGI
- small Peyer's patches / MGI
- decreased germinal center B cell number / MGI
- decreased spleen germinal center number / MGI
- decreased spleen germinal center size / MGI
- decreased IgG1 level / MGI
- decreased IgG2a level / MGI
- decreased IgG2b level / MGI
- increased IgG3 level / MGI
- decreased interferon-gamma secretion / MGI
- abnormal interleukin secretion / MGI
- decreased circulating interferon-gamma level / MGI
- decreased circulating interleukin-4 level / MGI
- decreased interleukin-4 secretion / MGI
- decreased interleukin-5 secretion / MGI
- abnormal interferon level / MGI
- abnormal interleukin level / MGI
- decreased IgG2c level / MGI
- decreased interleukin-21 secretion / MGI
- decreased pancreatic islet number / MGI
- abnormal NK cell physiology / MGI
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