B6Dnk;B6Brd;B6N-Tyrc-Brd Ctcftm1a(EUCOMM)Wtsi/WtsiH

Status

Available to order

EMMA IDEM:05852
International strain nameB6Dnk;B6Brd;B6N-Tyrc-Brd Ctcftm1a(EUCOMM)Wtsi/WtsiH
Alternative nameEPD0028_4_B04
Strain typeTargeted Mutant Strains
Allele/Transgene symbolCtcftm1a(EUCOMM)Wtsi
Gene/Transgene symbolCtcf
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 EPD0028_4_B04. 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
Breeding at archiving centreReceived as frozen sperm. May be carrying C57BL/6J-Tyrc-Brd and therefore potentially produce albino pups if intercrossed.

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

    • Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome / Orphanet_363611
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
  • embryonic growth arrest / MGI
  • absent inner cell mass / MGI
  • embryonic lethality at implantation / MGI
  • postnatal lethality, incomplete penetrance / MGI
  • embryonic lethality during organogenesis, complete penetrance / MGI
  • absent trophectoderm / MGI
  • increased embryonic tissue cell apoptosis / 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)
MTA will be issued after an order has been submitted.

EMMA conditions
Legally binding conditions for the transfer

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