C57BL/6N-Daam2tm1b(KOMP)Wtsi/H

Status

Only small colony available

EMMA IDEM:16271
Citation informationRRID:IMSR_EM:16271 

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-Daam2tm1b(KOMP)Wtsi/H
Alternative nameEPD0660_3_A09
Strain typeTargeted Mutant Strains
Allele/Transgene symbolDaam2tm1b(KOMP)Wtsi
Gene/Transgene symbolDaam2
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 Mary Lyon Centre at MRC Harwell
Provider affiliationMary Lyon Centre at MRC Harwell
Genetic informationThis mouse line originates from KOMP ES clone EPD0660_3_A09. 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. Click here for more information on KOMP final vectors.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (allele matching)
  • abnormal snout morphology / IMPC
  • abnormal maxilla morphology / IMPC
  • increased circulating phosphate level / IMPC
  • increased circulating alanine transaminase level / IMPC
  • increased circulating aspartate transaminase level / IMPC
  • increased hemoglobin content / IMPC
  • increased circulating amylase level / IMPC
  • increased large unstained cell number / IMPC
IMPC phenotypes (gene matching)
  • increased circulating alkaline phosphatase level / IMPC
  • abnormal snout morphology / IMPC
  • increased circulating alanine transaminase level / IMPC
  • abnormal maxilla morphology / IMPC
  • increased hemoglobin content / IMPC
  • abnormal cranium morphology / IMPC
  • increased circulating phosphate level / IMPC
  • increased fasting circulating glucose level / IMPC
  • developmental and structural abnormality / IMPC
  • decreased body length / IMPC
  • increased large unstained cell number / IMPC
  • increased circulating aspartate transaminase level / IMPC
  • increased circulating amylase level / IMPC

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Order (limited)

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*

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

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

Material Transfer Agreement (MTA)
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Legally binding conditions for the transfer

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