C57BL/6N-Nrastm1a(EUCOMM)Hmgu/H

Status

Available to order

EMMA IDEM:10426
Citation informationRRID:IMSR_EM:10426 

Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information.

 
International strain nameC57BL/6N-Nrastm1a(EUCOMM)Hmgu/H
Alternative nameHEPD0719_5_C04
Strain typeTargeted Mutant Strains
Allele/Transgene symbolNrastm1a(EUCOMM)Hmgu
Gene/Transgene symbolNras
DisclaimerPlease note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
  1. We can not guarantee a null mutation for Knock-out first alleles (tm1a alleles, see http://www.mousephenotype.org/about-ikmc/targeting-strategies) as the critical exon has not been deleted.
  2. That the structure of the targeted mutation in the ES cells obtained from EUCOMM/KOMP to generate EUCOMM/KOMP mice is not verified by INFRAFRONTIER/EMMA. It is recommended that the recipient confirms the mutation structure.
  3. No check for determining the copy number of the targeting construct in ES cells obtained from EUCOMM/KOMP is done by INFRAFRONTIER/EMMA.
  4. The level of quality control before mice are released is to confirm the individual mouse genotype by short range PCR.

Information from provider

Provider MRC, Medical Research Council
Provider affiliationMary Lyon Centre at MRC Harwell
Genetic informationThis mouse line originates from EUCOMM ES clone HEPD0719_5_C04. For further details on the construction of this clone see the page at the IKMC portal.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

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

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • preweaning lethality, complete penetrance / IMPC
  • increased circulating glucose level / IMPC
  • increased circulating HDL cholesterol level / IMPC
  • short tibia / IMPC
MGI phenotypes (gene matching)
  • abnormal leukocyte cell number / MGI
  • decreased monocyte cell number / MGI
  • increased granulocyte number / MGI
  • pale liver / MGI
  • abnormal thymus morphology / MGI
  • decreased body weight / MGI
  • weight loss / MGI
  • postnatal growth retardation / MGI
  • no abnormal phenotype detected / MGI
  • no phenotypic analysis / MGI
  • decreased spleen weight / MGI
  • increased T cell number / MGI
  • abnormal granulocyte differentiation / MGI
  • preweaning lethality, complete penetrance / MGI
  • chylous ascites / MGI

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Availabilities

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

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

Genotyping protocol

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

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