C3H.Cg-Fbxo11Jf/H

Status

Available to order

EMMA IDEM:00375
International strain nameC3H.Cg-Fbxo11Jf/H
Alternative nameJeff
Strain typeInduced Mutant Strains : Chemically-induced
Allele/Transgene symbolFbxo11Jf
Gene/Transgene symbolFbxo11

Information from provider

ProviderRachel Hardisty
Provider affiliationMRC Harwell, Didcot, Oxon, OX11 0RD
Phenotypic informationMice carrying this mutation are small with a short face and are deaf.
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;; 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

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Disease and phenotype information

MGI allele-associated human disease models

IMPC phenotypes (allele matching)
  • 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
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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Availabilities

Requesting frozen sperm or embryos is generally advisable wherever possible, in order to minimise the shipment of live mice.

  • Frozen embryos. Delivered in 4 weeks (after paperwork in place). €1740*
  • Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740*
  • Rederivation of mice from frozen stock, delivery time available upon request . €3880*
  • Tissue - Types of tissue, service fee and delivery time available upon request

Due to the dynamic nature of our processes strain availability may change at short notice. The local repository manager will advise you in these circumstances.

* In addition users have to cover all the shipping costs (including the cost for returning dry-shippers, where applicable).

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Practical information

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