C57BL/6N-Atm1Brd Myo10tm2(KOMP)Wtsi/WtsiOrl

Status

Available to order

EMMA IDEM:08386
Citation informationRRID:IMSR_EM:08386 

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-Atm1Brd Myo10tm2(KOMP)Wtsi/WtsiOrl
Alternative nameEPD0272_4_F10
Strain type
Allele/Transgene symbolMyo10tm2(KOMP)Wtsi
Gene/Transgene symbolMyo10
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 EPD0272_4_F10. 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/6NTac males

Disease and phenotype information

IMPC phenotypes (allele matching)
  • persistence of hyaloid vascular system / IMPC
  • abnormal lens morphology / IMPC
  • cataract / IMPC
  • fused cornea and lens / IMPC
  • abnormal cornea morphology / IMPC
  • corneal opacity / IMPC
  • abnormal iris morphology / IMPC
  • abnormal retina morphology / IMPC
  • abnormal response to new environment / IMPC
  • abnormal coat/hair pigmentation / IMPC
  • abnormal digit morphology / IMPC
  • abnormal tail morphology / IMPC
  • decreased circulating creatinine level / IMPC
  • impaired pupillary reflex / IMPC
  • fused phalanges / IMPC
IMPC phenotypes (gene matching)
  • abnormal retina morphology / IMPC
  • abnormal lens morphology / IMPC
  • abnormal coat/hair pigmentation / IMPC
  • abnormal digit morphology / IMPC
  • fused phalanges / IMPC
  • cataract / IMPC
  • fused cornea and lens / IMPC
  • abnormal cornea morphology / IMPC
  • corneal opacity / IMPC
  • abnormal tail morphology / IMPC
  • abnormal response to new environment / IMPC
  • persistence of hyaloid vascular system / IMPC
  • decreased circulating creatinine level / IMPC
  • abnormal iris morphology / IMPC
  • impaired pupillary reflex / IMPC
MGI phenotypes (gene matching)
  • belly spot / MGI
  • syndactyly / MGI
  • kinked tail / MGI
  • exencephaly / MGI
  • decreased body weight / MGI
  • decreased body size / MGI
  • persistence of hyaloid vascular system / MGI
  • anophthalmia / MGI
  • microphthalmia / MGI
  • corneal opacity / MGI
  • abnormal retina morphology / MGI
  • decreased embryo size / MGI
  • hemorrhage / MGI
  • abnormal eye morphology / MGI
  • abnormal brain morphology / MGI
  • no abnormal phenotype detected / MGI
  • abnormal retinal vasculature morphology / MGI
  • white spotting / MGI
  • acrania / MGI
  • abnormal vascular branching morphogenesis / MGI
  • abnormal tail pigmentation / MGI
  • behavior/neurological phenotype / MGI
  • abnormal lens development / MGI
  • fused phalanges / MGI
  • decreased survivor rate / MGI
  • craniorachischisis / MGI
  • failure of eyelid fusion / MGI
  • iris coloboma / MGI
  • lethality during fetal growth through weaning, incomplete penetrance / MGI
  • decreased tail pigmentation / MGI
  • absent liver / 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.

  • 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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