- 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 |
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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