- preweaning lethality, incomplete penetrance / IMPC
C57BL/6N-Atm1Brd Celf2tm1a(EUCOMM)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:10866 |
Citation information | RRID:IMSR_EM:10866 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/6N-Atm1Brd Celf2tm1a(EUCOMM)Wtsi/WtsiOulu |
Alternative name | EPD0423_4_B02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Celf2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Celf2 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0423_4_B02. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Non-specific early-onset epileptic encephalopathy / Orphanet_442835
IMPC phenotypes (gene matching)
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