C3;C-GckGena348/H

Status

Available to order

EMMA IDEM:01842
International strain nameC3;C-GckGena348/H
Alternative nameGck
Strain typeInduced Mutant Strains : Chemically-induced
Allele/Transgene symbolGckGena348
Gene/Transgene symbolGck

Information from provider

ProviderRoger Cox
Provider affiliationMRC Harwell, Didcot, Oxon
Genetic informationImpaired glucose tolerance in males and females
Phenotypic informationHigh blood glucose and increased body weight
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
  • A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.;Toye Ayo A, Moir Lee, Hugill Alison, Bentley Liz, Quarterman Julie, Mijat Vesna, Hough Tertius, Goldsworthy Michelle, Haynes Alison, Hunter A Jacqueline, Browne Mick, Spurr Nigel, Cox Roger D, ;2004;Diabetes;53;1577-83; 15161764

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

IMPC phenotypes (gene matching)
  • impaired glucose tolerance / IMPC
  • increased circulating glucose level / IMPC
  • increased circulating alkaline phosphatase level / IMPC
  • increased circulating fructosamine level / IMPC
  • preweaning lethality, incomplete penetrance / IMPC
  • increased fasting circulating glucose level / IMPC
MGI phenotypes (allele matching)
  • increased body weight / MGI
  • hyperglycemia / MGI
  • impaired glucose tolerance / MGI
MGI phenotypes (gene matching)
  • abnormal circulating cholesterol level / MGI
  • hypoglycemia / MGI
  • increased body weight / MGI
  • decreased body weight / MGI
  • increased circulating triglyceride level / MGI
  • increased circulating free fatty acid level / MGI
  • hyperglycemia / MGI
  • abnormal circulating insulin level / MGI
  • postnatal growth retardation / MGI
  • increased urine glucose level / MGI
  • abnormal glucose homeostasis / MGI
  • increased circulating insulin level / MGI
  • postnatal lethality / MGI
  • increased circulating ketone body level / MGI
  • hepatic steatosis / MGI
  • decreased circulating insulin level / MGI
  • decreased insulin secretion / MGI
  • abnormal pancreatic beta cell physiology / MGI
  • abnormal insulin secretion / MGI
  • abnormal pancreatic islet morphology / MGI
  • abnormal pancreatic beta cell morphology / MGI
  • impaired glucose tolerance / MGI
  • insulin resistance / MGI
  • homeostasis/metabolism phenotype / MGI
  • endocrine/exocrine gland phenotype / MGI
  • decreased glycogen level / MGI
  • increased circulating glucose level / MGI
  • decreased circulating glucose level / MGI
  • increased glycosylated hemoglobin level / MGI
  • decreased pancreatic beta cell mass / MGI
  • small pancreatic islets / MGI
  • mortality/aging / MGI
  • postnatal lethality, complete penetrance / MGI
  • embryonic lethality during organogenesis, incomplete penetrance / MGI
  • decreased glucokinase activity / 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
  • A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.;Toye Ayo A, Moir Lee, Hugill Alison, Bentley Liz, Quarterman Julie, Mijat Vesna, Hough Tertius, Goldsworthy Michelle, Haynes Alison, Hunter A Jacqueline, Browne Mick, Spurr Nigel, Cox Roger D, ;2004;Diabetes;53;1577-83; 15161764

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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*
  • 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).

More details on pricing and delivery times

Practical information

Example health report
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