- 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 |
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:
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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 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
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