- preweaning lethality, incomplete penetrance / IMPC
C57BL/6N-Celf2tm1c(EUCOMM)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:14327 |
Citation information | RRID:IMSR_EM:14327 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-Celf2tm1c(EUCOMM)Wtsi/WtsiPh |
Alternative name | EPD0423_4_B02 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Celf2tm1c(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 line originates from EUCOMM ES clone EPD0423_4_B02, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
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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