C57BL/6N-Cib2tm1a(EUCOMM)Wtsi/H

Status

Available to order

EMMA IDEM:05417
Citation informationRRID:IMSR_EM:05417 

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-Cib2tm1a(EUCOMM)Wtsi/H
Alternative nameEPD0337_2_D04
Strain typeTargeted Mutant Strains
Allele/Transgene symbolCib2tm1a(EUCOMM)Wtsi
Gene/Transgene symbolCib2
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 EPD0337_2_D04. For further details on the construction of this clone see the page at the IMPC portal.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom
Animals used for archivingheterozygous C57BL/6NTac males
Breeding at archiving centreChimeras were mated to C57BL/6N Tac USA and maintained on this background thereafter.

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • increased circulating cholesterol level / IMPC
  • abnormal ear morphology / IMPC
  • limb grasping / IMPC
  • decreased prepulse inhibition / IMPC
  • abnormal startle reflex / IMPC
  • increased circulating HDL cholesterol level / IMPC
  • increased basophil cell number / IMPC
  • abnormal auditory brainstem response / IMPC
  • tremors / IMPC
  • increased circulating triglyceride level / IMPC
  • decreased startle reflex / IMPC
  • increased circulating fructosamine level / IMPC
MGI phenotypes (gene matching)
  • abnormal hearing physiology / MGI
  • deafness / MGI
  • abnormal cochlear hair cell morphology / MGI
  • cochlear hair cell degeneration / MGI
  • absent cochlear microphonics / MGI
  • abnormal hair cell mechanoelectric transduction / MGI
  • absent distortion product otoacoustic emissions / MGI
  • vision/eye phenotype / MGI
  • increased or absent threshold for auditory brainstem response / MGI

Information on how we integrate external resources can be found here

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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
(Current health report will be provided later)

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

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Legally binding conditions for the transfer

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