- increased leukocyte cell number / MGI
- decreased cell proliferation / MGI
- hindlimb paralysis / MGI
- increased inferior colliculus size / MGI
- decreased corpus callosum size / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal stratification in cerebral cortex / MGI
- abnormal hippocampus morphology / MGI
- abnormal cerebellum morphology / MGI
- increased superior colliculus size / MGI
- abnormal posture / MGI
- decreased embryo size / MGI
- embryonic growth arrest / MGI
- hydroencephaly / MGI
- abnormal developmental patterning / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal brain morphology / MGI
- abnormal chorion morphology / MGI
- vertebral transformation / MGI
- spina bifida / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- cervical vertebral transformation / MGI
- lumbar vertebral transformation / MGI
- thoracic vertebral transformation / MGI
- increased lymphocyte cell number / MGI
- abnormal amnion morphology / MGI
- thrombocytosis / MGI
- enlarged tectum / MGI
- increased histiocytic sarcoma incidence / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality between somite formation and embryo turning, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- abnormal amniotic cavity morphology / MGI
- abnormal extraembryonic coelom morphology / MGI
- abnormal ectoplacental cavity morphology / MGI
- diastematomyelia / MGI
- increased embryonic tissue cell apoptosis / MGI
C57BL/6NCrl-Suz12em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:15161 |
Citation information | RRID:IMSR_EM:15161 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-Suz12em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Suz12em1(IMPC)Ccpcz |
Gene/Transgene symbol | Suz12 |
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
- Weaver syndrome / Orphanet_3447
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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