B6NCrl;B6N-Bnc2tm1a(KOMP)Wtsi/Orl

Status

Available to order

EMMA IDEM:10945
Citation informationRRID:IMSR_EM:10945 

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 nameB6NCrl;B6N-Bnc2tm1a(KOMP)Wtsi/Orl
Alternative nameEPD0025_5_G05
Strain typeTargeted Mutant Strains
Allele/Transgene symbolBnc2tm1a(KOMP)Wtsi
Gene/Transgene symbolBnc2
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 Institut de Transgenose, INTRAGENE
Provider affiliationTAAM-CDTA UPS44, Institut de Transgenose, INTRAGENE
Genetic informationThis mouse line originates from KOMP ES clone EPD0025_5_G05. 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 centreInstitut de Transgenose, INTRAGENE, Orléans, France
Animals used for archivingheterozygous C57BL/6NCrl males

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • decreased fluid intake / IMPC
  • decreased exploration in new environment / IMPC
  • increased cornea thickness / IMPC
MGI phenotypes (gene matching)
  • microcephaly / MGI
  • parietal bone hypoplasia / MGI
  • abnormal pterygoid process morphology / MGI
  • small alisphenoid bone / MGI
  • absent palatine bone / MGI
  • abnormal maxillary shelf morphology / MGI
  • frontal bone hypoplasia / MGI
  • meteorism / MGI
  • abnormal palate development / MGI
  • decreased birth body size / MGI
  • palatal shelves fail to meet at midline / MGI
  • cleft secondary palate / MGI
  • decreased tongue size / MGI
  • neonatal lethality, complete penetrance / MGI
  • wide sagittal suture / MGI
  • large posterior fontanelle / MGI

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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