- increased mean platelet volume / IMPC
C57BL/6N-Cpt1atm1.2(IMPC)Wtsi/WtsiCnrm
Status | Available to order |
EMMA ID | EM:13412 |
Citation information | RRID:IMSR_EM:13412 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-Cpt1atm1.2(IMPC)Wtsi/WtsiCnrm |
Alternative name | Cpt1a_65_B04 |
Strain type | |
Allele/Transgene symbol | Cpt1atm1.2(IMPC)Wtsi |
Gene/Transgene symbol | Cpt1a |
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 undef ES clone Cpt1a_65_B04. For further details on the construction of this clone see the page at the IMPC portal. ES cells were generated using the CRISPR/Cas9 technology. The details of the applied experimental procedures involving CRISPR/Cas9 technology are not available. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Carnitine palmitoyl transferase 1A deficiency / Orphanet_156
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased mean platelet volume / IMPC
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