C57BL/6N-Atm1Brd Dsc2tm1e(KOMP)Wtsi/WtsiIeg

Status

Available to order

EMMA IDEM:13993
International strain nameC57BL/6N-Atm1Brd Dsc2tm1e(KOMP)Wtsi/WtsiIeg
Alternative nameEPD0567_2_H12
Strain typeTargeted Mutant Strains : Targeted Non-conditional
Allele/Transgene symbolDsc2tm1e(KOMP)Wtsi
Gene/Transgene symbolDsc2
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 Wellcome Trust Sanger Institute
Provider affiliationWellcome Trust Sanger Institute
Genetic informationThis mouse line originates from KOMP ES clone EPD0567_2_H12. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. Click here for more information on KOMP final vectors.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

    • Hereditary hypotrichosis with recurrent skin vesicles / Orphanet_217407
    • Familial isolated arrhythmogenic ventricular dysplasia, right dominant form / Orphanet_293910
    • Familial isolated arrhythmogenic ventricular dysplasia, biventricular form / Orphanet_293899
    • Familial isolated arrhythmogenic ventricular dysplasia, left dominant form / Orphanet_293888
IMPC phenotypes (allele matching)
  • abnormal cornea morphology / IMPC
  • corneal opacity / IMPC
  • narrow eye opening / IMPC
  • corneal vascularization / IMPC
IMPC phenotypes (gene matching)
  • corneal vascularization / IMPC
  • corneal opacity / IMPC
  • narrow eye opening / IMPC
  • abnormal cornea morphology / IMPC

Information on how we integrate external resources can be found here

Order

Availabilities

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

  • Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740*
  • Rederivation of mice from frozen stock, delivery time available upon request . €3880*

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

Genotyping protocol

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

Material Transfer Agreement (MTA)
Distribution of this strain is subject to a provider MTA. Both signing of the MTA and submission of the online EMMA Mutant Request Form are required before material can be shipped.

EMMA conditions
Legally binding conditions for the transfer

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