- 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 |
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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