- abnormal microglial cell morphology / MGI
- abnormal immune system cell morphology / MGI
- abnormal corpus callosum morphology / MGI
- thickened cerebral cortex / MGI
- abnormal hippocampus morphology / MGI
- abnormal CNS glial cell morphology / MGI
- hypoactivity / MGI
- decreased IgG level / MGI
- increased dopamine level / MGI
- abnormal B cell differentiation / MGI
- increased brain weight / MGI
- abnormal macrophage physiology / MGI
- increased IgM level / MGI
- increased IgA level / MGI
- abnormal neuron morphology / MGI
- nervous system phenotype / MGI
- abnormal nucleus accumbens morphology / MGI
- abnormal B cell morphology / MGI
- decreased B-1 B cell number / MGI
- decreased susceptibility to parasitic infection / MGI
- decreased B cell proliferation / MGI
- abnormal T cell proliferation / MGI
- increased B cell proliferation / MGI
- abnormal T-helper 2 physiology / MGI
- decreased susceptibility to type I hypersensitivity reaction / MGI
- decreased B-1a cell number / MGI
- abnormal hippocampus CA1 region morphology / MGI
- decreased IgG1 level / MGI
- increased IgG3 level / MGI
- impaired behavioral response to cocaine / MGI
- abnormal hippocampus pyramidal cell morphology / MGI
- increased astrocyte number / MGI
- increased hippocampus volume / MGI
C57BL/6NCrl-Cd81em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:13052 |
Citation information | RRID:IMSR_EM:13052 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-Cd81em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Cd81em1(IMPC)Ccpcz |
Gene/Transgene symbol | Cd81 |
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
- Common variable immunodeficiency / Orphanet_1572
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).