C3H.C-MecomJbo/H

Status

Available to order

EMMA IDEM:00091
International strain nameC3H.C-MecomJbo/H
Alternative nameGENA251
Strain typeInduced Mutant Strains : Chemically-induced
Allele/Transgene symbolMecomJbo,
Gene/Transgene symbolMecom

Information from provider

ProviderNick Parkinson
Provider affiliationMRC Mammalian Genetics Unit
Phenotypic informationThese mice have late onset deafness, an extra digit, reduced body weight and craniofacial defects
References
  • A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.;Nolan P M, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray I C, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson J A, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel K P, Voegeling S, Guenet J L, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher E M, Martin J, Rastan S, Brown S D, Hunter J, ;2000;Nature genetics;25;440-3; 10932191
  • Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media.;Parkinson Nicholas, Hardisty-Hughes Rachel E, Tateossian Hilda, Tsai Hsun-Tien, Brooker Debra, Morse Sue, Lalane Zuzanna, MacKenzie Francesca, Fray Martin, Glenister Pete, Woodward Anne-Marie, Polley Sian, Barbaric Ivana, Dear Neil, Hough Tertius A, Hunter A Jackie, Cheeseman Michael T, Brown Steve D M, ;2006;PLoS genetics;2;e149; 17029558

Information from EMMA

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

Disease and phenotype information

MGI allele-associated human disease models

Orphanet associated rare diseases, based on orthologous gene matching

    • Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome / Orphanet_71289
IMPC phenotypes (allele matching)
  • decreased hematocrit / IMPC
  • decreased body weight / IMPC
  • abnormal startle reflex / IMPC
  • increased startle reflex / IMPC
  • limb grasping / IMPC
  • decreased hemoglobin content / IMPC
  • decreased erythrocyte cell number / IMPC
  • abnormal locomotor activation / IMPC
  • increased lean body mass / IMPC
  • decreased circulating iron level / IMPC
  • increased blood urea nitrogen level / IMPC
  • increased circulating amylase level / IMPC
  • decreased prepulse inhibition / IMPC
  • increased total body fat amount / IMPC
MGI phenotypes (allele matching)
  • abnormal craniofacial morphology / MGI
  • polydactyly / MGI
  • decreased body weight / MGI
  • increased susceptibility to otitis media / MGI
  • deafness / MGI
  • respiratory system inflammation / MGI
  • abnormal neutrophil differentiation / MGI
  • abnormal miscarriage rate / MGI
  • immune system phenotype / MGI
  • abnormal tympanic membrane morphology / MGI
  • tympanic membrane perforation / MGI
  • abnormal pinna reflex / MGI
  • hearing/vestibular/ear phenotype / MGI
  • impaired hearing / MGI
  • middle ear polyps / MGI
  • middle ear effusion / MGI
  • distended pericardium / MGI
  • abnormal forebrain morphology / MGI
  • brachydactyly / MGI
  • abnormal limb development / MGI
  • perinatal lethality, incomplete penetrance / MGI
  • embryonic lethality during organogenesis, incomplete penetrance / MGI
  • perinatal lethality, complete penetrance / MGI

Literature references

  • A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.;Nolan P M, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray I C, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson J A, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel K P, Voegeling S, Guenet J L, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher E M, Martin J, Rastan S, Brown S D, Hunter J, ;2000;Nature genetics;25;440-3; 10932191
  • Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media.;Parkinson Nicholas, Hardisty-Hughes Rachel E, Tateossian Hilda, Tsai Hsun-Tien, Brooker Debra, Morse Sue, Lalane Zuzanna, MacKenzie Francesca, Fray Martin, Glenister Pete, Woodward Anne-Marie, Polley Sian, Barbaric Ivana, Dear Neil, Hough Tertius A, Hunter A Jackie, Cheeseman Michael T, Brown Steve D M, ;2006;PLoS genetics;2;e149; 17029558

Order

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*

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).

More details on pricing and delivery times

Practical information

Example health report
(Current health report will be provided later)

Material Transfer Agreement (MTA)
MTA will be issued after an order has been submitted.

EMMA conditions
Legally binding conditions for the transfer

Other EMMA strains

Not found what you were looking for? Search here for other strains available from EMMA.


Search
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).