- abnormal cerebellar granule layer morphology / MGI
- abnormal trigeminal nerve morphology / MGI
- abnormal lipid homeostasis / MGI
- abnormal hippocampal fimbria morphology / MGI
- increased hepatocellular carcinoma incidence / MGI
- abnormal myelin sheath morphology / MGI
- increased liver tumor incidence / MGI
- abnormal brain white matter morphology / MGI
- integument phenotype / MGI
B6;129S4-Cers2Gt(S16-4B1)Sor/Cnrm
Status | Available to order |
EMMA ID | EM:04933 |
Citation information | RRID:IMSR_EM:04933 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 | B6;129S4-Cers2Gt(S16-4B1)Sor/Cnrm |
Alternative name | CerS2 gene trap |
Strain type | Gene-trap |
Allele/Transgene symbol | Cers2Gt(S16-4B1)Sor |
Gene/Transgene symbol | Cers2 |
Information from provider
Provider | Klaus WILLECKE |
Provider affiliation | Molekulargenetik, Institut fuer Genetik, Universitaet Bonn |
Genetic information | A gene-trap (Rosafary) is inserted into intron 1 of Cers2 (Lass2), leading to the disruption of Cers2 expression. Instead, a lacZ reporter gene is expressed under control of the Cers2 promoter. The hygromycin resistance cassette was removed via flp recombinase-mediated recombination. |
Phenotypic information | Adult homozygous Cers2 gene-trap mice are smaller than their wild-type littermates. They develop liver carcinomas and show myelin degeneration. |
Breeding history | The first heterozygous offspring of chimeras were backcrossed three times with C57BL/6. Cers2 gene-trap mice are currently mated to C57BL/6 or inbred. |
References |
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Homozygous fertile | not known |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal cerebellar granule layer morphology / MGI
- abnormal trigeminal nerve morphology / MGI
- abnormal lipid homeostasis / MGI
- abnormal hippocampal fimbria morphology / MGI
- increased hepatocellular carcinoma incidence / MGI
- abnormal myelin sheath morphology / MGI
- increased liver tumor incidence / MGI
- abnormal brain white matter morphology / MGI
- integument phenotype / MGI
Literature references
- Adult ceramide synthase 2 (CERS2)-deficient mice exhibit myelin sheath defects, cerebellar degeneration, and hepatocarcinomas.;Imgrund Silke, Hartmann Dieter, Farwanah Hany, Eckhardt Matthias, Sandhoff Roger, Degen Joachim, Gieselmann Volkmar, Sandhoff Konrad, Willecke Klaus, ;2009;The Journal of biological chemistry;284;33549-60; 19801672
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