- decreased bone marrow cell number / MGI
- decreased cell proliferation / MGI
- abnormal immune system morphology / MGI
- small spleen / MGI
- abnormal thymus morphology / MGI
- small thymus / MGI
- decreased thymocyte number / MGI
- abnormal immune system cell morphology / MGI
- abnormal lymphocyte cell number / MGI
- absent CD8-positive, alpha-beta T cells / MGI
- abnormal diencephalon morphology / MGI
- decreased body weight / MGI
- decreased body size / MGI
- postnatal growth retardation / MGI
- abnormal immune system physiology / MGI
- arrested B cell differentiation / MGI
- decreased IgG level / MGI
- decreased IgM level / MGI
- decreased IgA level / MGI
- arrested T cell differentiation / MGI
- abnormal T cell activation / MGI
- intestinal inflammation / MGI
- liver inflammation / MGI
- reduced fertility / MGI
- increased cellular sensitivity to gamma-irradiation / MGI
- increased T cell derived lymphoma incidence / MGI
- premature death / MGI
- abnormal B cell differentiation / MGI
- abnormal T cell differentiation / MGI
- abnormal lymphopoiesis / MGI
- abnormal proerythroblast morphology / MGI
- decreased immunoglobulin level / MGI
- abnormal immune system organ morphology / MGI
- increased neuron apoptosis / MGI
- chromosome breakage / MGI
- spontaneous chromosome breakage / MGI
- induced chromosome breakage / MGI
- abnormal striatum morphology / MGI
- decreased fetal size / MGI
- increased cellular sensitivity to ionizing radiation / MGI
- increased anti-double stranded DNA antibody level / MGI
- decreased hematopoietic stem cell number / MGI
- increased anti-chromatin antibody level / MGI
- abnormal regulatory T cell morphology / MGI
- decreased spleen weight / MGI
- decreased thymus weight / MGI
- decreased lymphocyte cell number / MGI
- decreased B cell number / MGI
- decreased double-negative T cell number / MGI
- decreased double-positive T cell number / MGI
- decreased T cell proliferation / MGI
- abnormal brainstem morphology / MGI
- cellular phenotype / MGI
- hematopoietic system phenotype / MGI
- abnormal cell physiology / MGI
- thin cerebral cortex / MGI
- increased medulloblastoma incidence / MGI
- increased T cell apoptosis / MGI
- abnormal DNA repair / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- abnormal B cell activation / MGI
- decreased IgG2b level / MGI
- decreased IgG3 level / MGI
- decreased interferon-gamma secretion / MGI
- decreased interleukin-13 secretion / MGI
- abnormal T cell receptor V(D)J recombination / MGI
- abnormal T cell receptor beta chain V(D)J recombination / MGI
- chromosomal instability / MGI
- increased colon adenocarcinoma incidence / MGI
- decreased splenocyte number / MGI
- prenatal lethality, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- decreased fibroblast proliferation / MGI
- increased forebrain apoptosis / MGI
- increased spinal cord apoptosis / MGI
C57BL/6NCrl-Lig4em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15733 |
Citation information | RRID:IMSR_EM:15733 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-Lig4em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Lig4em1(IMPC)Ccpcz |
Gene/Transgene symbol | Lig4 |
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
- Omenn syndrome / Orphanet_39041
- LIG4 syndrome / Orphanet_99812
- Dubowitz syndrome / Orphanet_235
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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