C57BL/6N-Lmnb1tm1c(EUCOMM)Wtsi/WtsiH

Status

Available to order

EMMA IDEM:10615
International strain nameC57BL/6N-Lmnb1tm1c(EUCOMM)Wtsi/WtsiH
Alternative nameEPD0070_1_G07
Strain typeTargeted Mutant Strains : Targeted Conditional
Allele/Transgene symbolLmnb1tm1c(EUCOMM)Wtsi
Gene/Transgene symbolLmnb1
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 line originates from EUCOMM ES clone EPD0070_1_G07, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 centreThis mutation was generated on a coisogenic C57BL/6NTac background

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • decreased body weight / IMPC
  • lipid deposition / IMPC
MGI phenotypes (gene matching)
  • delayed bone ossification / MGI
  • scoliosis / MGI
  • decreased circulating calcium level / MGI
  • decreased cell proliferation / MGI
  • microcephaly / MGI
  • abnormal cranium morphology / MGI
  • thin diaphragm muscle / MGI
  • decreased brain size / MGI
  • abnormal stratification in cerebral cortex / MGI
  • abnormal lung morphology / MGI
  • abnormal lung development / MGI
  • absent pulmonary alveoli / MGI
  • decreased body weight / MGI
  • decreased embryo size / MGI
  • respiratory failure / MGI
  • abnormal pulmonary alveolus morphology / MGI
  • abnormal neuron morphology / MGI
  • decreased circulating alkaline phosphatase level / MGI
  • abnormal thoracic vertebrae morphology / MGI
  • abnormal cell nucleus morphology / MGI
  • abnormal coronal suture morphology / MGI
  • abnormal sagittal suture morphology / MGI
  • decreased fetal size / MGI
  • abnormal neuronal precursor proliferation / MGI
  • abnormal cell differentiation / MGI
  • increased mean corpuscular hemoglobin / MGI
  • abnormal neuronal migration / MGI
  • impaired lung alveolus development / MGI
  • neonatal lethality, complete penetrance / MGI
  • abnormal phrenic nerve innervation pattern to diaphragm / MGI
  • decreased midbrain size / MGI
  • flat head / MGI

Information on how we integrate external resources can be found here

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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).

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Practical information

Genotyping protocol

Example health report
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Material Transfer Agreement (MTA)
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