- decreased leukocyte cell number / IMPC
- decreased circulating iron level / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- thrombocytosis / IMPC
- hyperplasia / IMPC
- atrophy / IMPC
- extramedullary hemopoiesis / IMPC
- decreased circulating fructosamine level / IMPC
- hypoplasia / IMPC
- increased circulating sodium level / IMPC
- increased mean corpuscular hemoglobin / IMPC
- male infertility / IMPC
- decreased hematocrit / IMPC
- increased red blood cell distribution width / IMPC
- process of degenerative change / IMPC
- increased circulating bilirubin level / IMPC
C57BL/6N-Fbxo7tm1c(EUCOMM)Wtsi/WtsiCnrm
Status | Available to order |
EMMA ID | EM:11752 |
Citation information | RRID:IMSR_EM:11752 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-Fbxo7tm1c(EUCOMM)Wtsi/WtsiCnrm |
Alternative name | EPD0622_3_D02 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Fbxo7tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Fbxo7 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This line originates from EUCOMM ES clone EPD0622_3_D02, 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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Parkinsonian-pyramidal syndrome / Orphanet_171695
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).