- decreased bone mineral density / IMPC
- abnormal retina morphology / IMPC
- hyperactivity / IMPC
- abnormal startle reflex / IMPC
- increased startle reflex / IMPC
- abnormal vocalization / IMPC
- decreased mean corpuscular volume / IMPC
- decreased circulating triglyceride level / IMPC
- decreased heart weight / IMPC
- abnormal bone mineralization / IMPC
- thrombocytopenia / IMPC
- abnormal locomotor activation / IMPC
- abnormal defecation / IMPC
- increased lean body mass / IMPC
- decreased lean body mass / IMPC
- decreased prepulse inhibition / IMPC
- increased total body fat amount / IMPC
- increased bone mineral content / IMPC
- preweaning lethality, complete penetrance / IMPC
C3H.Cg-Fbxo11Jf/H
Status | Available to order |
EMMA ID | EM:00375 |
International strain name | C3H.Cg-Fbxo11Jf/H |
Alternative name | Jeff |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Fbxo11Jf |
Gene/Transgene symbol | Fbxo11 |
Information from provider
Provider | Rachel Hardisty |
Provider affiliation | MRC Harwell, Didcot, Oxon, OX11 0RD |
Phenotypic information | Mice carrying this mutation are small with a short face and are deaf. |
References |
|
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- 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
MGI phenotypes (allele matching)
- short snout / MGI
- decreased body weight / MGI
- decreased body size / 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
- absent pinna reflex / MGI
- abnormal tympanic cavity morphology / MGI
- middle ear polyps / MGI
- middle ear effusion / MGI
- tympanic membrane retraction / MGI
- excessive cerumen / MGI
- abnormal pinna reflex / MGI
- impaired hearing / MGI
- midline facial cleft / MGI
- cleft palate / MGI
- eyelids open at birth / MGI
- neonatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- short face / MGI
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
Literature references
- A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment.;Hardisty-Hughes Rachel E, Parker Andrew, Brown Steve D M, ;2010;Nature protocols;5;177-90; 20057387
- A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.;Hardisty-Hughes Rachel E, Tateossian Hilda, Morse Susan A, Romero M Rosario, Middleton Alice, Tymowska-Lalanne Zuzanna, Hunter A Jackie, Cheeseman Michael, Brown Steve D M, ;2006;Human molecular genetics;15;3273-9; 17035249
- Chronic otitis media is initiated by a bulla cavitation defect in the FBXO11 mouse model.;Del-Pozo Jorge, MacIntyre Neil, Azar Ali, Glover James, Milne Elspeth, Cheeseman Michael, ;2019;Disease models & mechanisms;12;985214; 30898767
- The EDA-deficient mouse has Zymbal's gland hypoplasia and acute otitis externa.;Del-Pozo Jorge, Headon Denis J, Glover James D, Azar Ali, Schuepbach-Mallepell Sonia, Bhutta Mahmood F, Riddell Jon, Maxwell Scott, Milne Elspeth, Schneider Pascal, Cheeseman Michael, ;2022;Disease models & mechanisms;15;; 35107126
- Trans-cortical vessels in the mouse temporal bulla bone are a means to recruit myeloid cells in chronic otitis media and limit peripheral leukogram changes.;Azar Ali, Bhutta Mahmood F, Del-Pozo Jorge, Milne Elspeth, Cheeseman Michael, ;2022;Frontiers in genetics;13;; 36246635
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