- 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 |
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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