C57BL/6N-Wactm2b(EUCOMM)Wtsi/WtsiCnbc

Status

Available to order

EMMA IDEM:14212
International strain nameC57BL/6N-Wactm2b(EUCOMM)Wtsi/WtsiCnbc
Alternative nameMEPD0997_2_D04
Strain typeTargeted Mutant Strains
Allele/Transgene symbolWactm2b(EUCOMM)Wtsi
Gene/Transgene symbolWac
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 EUCOMM ES clone MEPD0997_2_D04. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele using a cell permeable HTN-Cre as described in doi:10.1007/s11248-013-9764-x. Click here for more information on EUCOMM final vectors.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreCNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain
Animals used for archivingheterozygous C57BL/6N

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

    • Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation / Orphanet_466950
IMPC phenotypes (allele matching)
  • increased monocyte cell number / IMPC
  • abnormal cranium morphology / IMPC
  • increased mean platelet volume / IMPC
  • decreased circulating triglyceride level / IMPC
  • increased circulating alkaline phosphatase level / IMPC
  • fusion of vertebral arches / IMPC
  • decreased eosinophil cell number / IMPC
  • decreased circulating amylase level / IMPC
  • preweaning lethality, complete penetrance / IMPC
  • increased Ly6C low monocyte number / IMPC
IMPC phenotypes (gene matching)
  • decreased eosinophil cell number / IMPC
  • increased Ly6C low monocyte number / IMPC
  • increased circulating alkaline phosphatase level / IMPC
  • abnormal cranium morphology / IMPC
  • decreased circulating triglyceride level / IMPC
  • fusion of vertebral arches / IMPC
  • preweaning lethality, complete penetrance / IMPC
  • decreased circulating amylase level / IMPC
  • increased monocyte cell number / IMPC
  • increased mean platelet volume / 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.

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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