- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Elac2tm1c(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:13457 |
Citation information | RRID:IMSR_EM:13457 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-Elac2tm1c(EUCOMM)Wtsi/WtsiBiat |
Alternative name | C57BL/6NTac-Elac2 tm1c(EUCOMM)Wtsi/WtsiBiat |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Elac2tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Elac2 |
Information from provider
Provider | Maik Dahlhoff |
Provider affiliation | Department of Biomedical Sciences, University of Veterinary Medicine |
Genetic information | This line originates from EMMA strain EM:05966, C57BL/6NTac-Elac2tm1a(EUCOMM)Wtsi/WtsiBiat (EUCOMM ES clone EPD0201_1_B07), 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 relevant page at the IMPC portal (https://www.mousephenotype.org/data/genes/MGI:1890496#order). |
Phenotypic information | Homozygous:No homozygous mice have been producedHeterozygous:No data available, no phenotype expected |
Breeding history | 1 backcross generation to C57BL/6N after flp-deleter breeding |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | no |
Information from EMMA
Archiving centre | University of Veterinary Medicine, Vienna, Austria |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Combined oxidative phosphorylation defect type 17 / Orphanet_369913
IMPC phenotypes (gene matching)
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