- no spontaneous movement / IMPC
- abnormal coat appearance / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal skin morphology / IMPC
- enlarged seminal vesicle / IMPC
- abnormal vertebral arch morphology / IMPC
- abnormal optic disk morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased Ly6C-positive mature NK cell number / IMPC
C57BL/6NCrl-Cluhem1(IMPC)Ccpcz/Ph
Status | Available to order |
EMMA ID | EM:11305 |
Citation information | RRID:IMSR_EM:11305 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-Cluhem1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Cluhem1(IMPC)Ccpcz |
Gene/Transgene symbol | Cluh |
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 |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal skin morphology / IMPC
- no spontaneous movement / IMPC
- enlarged seminal vesicle / IMPC
- abnormal coat appearance / IMPC
- abnormal optic disk morphology / IMPC
- increased Ly6C-positive mature NK cell number / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal vertebral arch morphology / IMPC
MGI phenotypes (gene matching)
- abnormal liver physiology / MGI
- decreased body weight / MGI
- abnormal homeostasis / MGI
- growth/size/body region phenotype / MGI
- embryo phenotype / MGI
- cellular phenotype / MGI
- respiratory system phenotype / MGI
- abnormal mitochondrion morphology / MGI
- decreased embryo weight / MGI
- mortality/aging / MGI
- abnormal tricarboxylic acid cycle / MGI
- neonatal lethality, complete penetrance / MGI
- abnormal mitochondrial matrix morphology / MGI
- decreased fasted circulating glucose level / MGI
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