- absent pre-B cells / MGI
- abnormal cell death / MGI
- increased cell proliferation / MGI
- abnormal immune system morphology / MGI
- enlarged thymus / MGI
- abnormal lymphocyte cell number / MGI
- decreased body size / MGI
- postnatal growth retardation / MGI
- arrested B cell differentiation / MGI
- thymus hypoplasia / MGI
- female infertility / MGI
- increased T cell derived lymphoma incidence / MGI
- postnatal lethality / MGI
- premature death / MGI
- abnormal B cell differentiation / MGI
- no abnormal phenotype detected / MGI
- abnormal hematopoietic system morphology/development / MGI
- abnormal lymphopoiesis / MGI
- abnormal blood cell morphology/development / MGI
- abnormal B cell number / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- spleen atrophy / MGI
- abnormal T cell subpopulation ratio / MGI
- abnormal hematopoietic stem cell morphology / MGI
- increased B cell number / MGI
- decreased lymphocyte cell number / MGI
- decreased B cell number / MGI
- increased double-negative T cell number / MGI
- decreased double-positive T cell number / MGI
- immune system phenotype / MGI
- reproductive system phenotype / MGI
- hematopoietic system phenotype / MGI
- decreased NK cell number / MGI
- absent B cells / MGI
- increased single-positive T cell number / MGI
- decreased dendritic cell number / MGI
- absent pro-B cells / MGI
- decreased pro-B cell number / MGI
- decreased pre-B cell number / MGI
- abnormal immunoglobulin V(D)J recombination / MGI
- abnormal immunoglobulin heavy chain V(D)J recombination / MGI
- abnormal immunoglobulin light chain V-J recombination / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
C57BL/6NCrl-Tcf3em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:14816 |
Citation information | RRID:IMSR_EM:14816 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-Tcf3em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Tcf3em1(IMPC)Ccpcz |
Gene/Transgene symbol | Tcf3 |
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
- Autosomal agammaglobulinemia / Orphanet_33110
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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