- decreased prepulse inhibition / IMPC
- increased lean body mass / IMPC
- decreased hematocrit / IMPC
- thrombocytopenia / IMPC
- decreased circulating iron level / IMPC
- decreased heart weight / IMPC
- increased total body fat amount / IMPC
- abnormal startle reflex / IMPC
- abnormal defecation / IMPC
- abnormal locomotor activation / IMPC
- increased startle reflex / IMPC
- hyperactivity / IMPC
- abnormal vocalization / IMPC
- decreased hemoglobin content / IMPC
- narrow eye opening / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased mean corpuscular volume / IMPC
- increased bone mineral content / IMPC
- decreased circulating calcium level / IMPC
- decreased lean body mass / IMPC
- decreased circulating triglyceride level / IMPC
- decreased circulating total protein level / IMPC
- decreased erythrocyte cell number / IMPC
- short tibia / IMPC
- abnormal retina morphology / IMPC
- increased fasting circulating glucose level / IMPC
- increased red blood cell distribution width / IMPC
- decreased bone mineral density / IMPC
- abnormal bone mineralization / IMPC
C57BL/6N-Fbxo11tm2a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:06999 |
Citation information | RRID:IMSR_EM:06999 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-Fbxo11tm2a(EUCOMM)Wtsi/H |
Alternative name | EPD0248_1_H03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Fbxo11tm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Fbxo11 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0248_1_H03. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- midline facial cleft / MGI
- cleft palate / MGI
- decreased hair follicle number / MGI
- short snout / MGI
- thick epidermis / MGI
- epidermal hyperplasia / MGI
- decreased body weight / MGI
- decreased body size / MGI
- eyelids open at birth / MGI
- abnormal pinna reflex / MGI
- decreased startle reflex / MGI
- increased susceptibility to otitis media / MGI
- deafness / MGI
- abnormal cytokine secretion / MGI
- abnormal auditory tube / MGI
- decreased endocochlear potential / MGI
- abnormal middle ear ossicle morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- impaired hearing / MGI
- absent pinna reflex / MGI
- abnormal protein level / MGI
- absent keratohyalin granules / MGI
- neonatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- short face / MGI
- abnormal tympanic cavity morphology / MGI
- middle ear polyps / MGI
- middle ear effusion / MGI
- tympanic membrane retraction / MGI
- excessive cerumen / MGI
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