C57BL/6NCrl-Erbb2tm1b(EUCOMM)Hmgu/Ieg

Status

Available to order

EMMA IDEM:12826
International strain nameC57BL/6NCrl-Erbb2tm1b(EUCOMM)Hmgu/Ieg
Alternative nameHEPD0668_3_H11
Strain typeTargeted Mutant Strains
Allele/Transgene symbolErbb2tm1b(EUCOMM)Hmgu
Gene/Transgene symbolErbb2
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 Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH)
Provider affiliationInstitute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH)
Genetic informationThis mouse line originates from EUCOMM ES clone HEPD0668_3_H11. 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 EUCOMM final vectors.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany
Animals used for archivingheterozygous C57BL/6N

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (allele matching)
  • preweaning lethality, complete penetrance / IMPC
IMPC phenotypes (gene matching)
  • preweaning lethality, complete penetrance / IMPC
MGI phenotypes (gene matching)
  • enlarged heart / MGI
  • thin ventricular wall / MGI
  • absent myocardial trabeculae / MGI
  • absent trabeculae carneae / MGI
  • decreased atrioventricular cushion size / MGI
  • abnormal motor neuron innervation pattern / MGI
  • abnormal oligodendrocyte morphology / MGI
  • abnormal dorsal root ganglion morphology / MGI
  • abnormal sensory neuron morphology / MGI
  • abnormal sensory neuron innervation pattern / MGI
  • absent primary muscle spindle / MGI
  • partial loss of secondary muscle spindle / MGI
  • abnormal sympathetic ganglion morphology / MGI
  • abnormal cranial nerve morphology / MGI
  • abnormal trigeminal nerve morphology / MGI
  • abnormal glossopharyngeal nerve morphology / MGI
  • abnormal vagus nerve morphology / MGI
  • abnormal hypoglossal nerve morphology / MGI
  • abnormal phrenic nerve morphology / MGI
  • defasiculated phrenic nerve / MGI
  • abnormal cranial ganglia morphology / MGI
  • abnormal geniculate ganglion morphology / MGI
  • abnormal petrosal ganglion morphology / MGI
  • abnormal trigeminal ganglion morphology / MGI
  • small superior vagus ganglion / MGI
  • cyanosis / MGI
  • poor circulation / MGI
  • irregular heartbeat / MGI
  • absent vitelline blood vessels / MGI
  • hemorrhage / MGI
  • respiratory failure / MGI
  • prenatal lethality / MGI
  • abnormal blood circulation / MGI
  • no abnormal phenotype detected / MGI
  • abnormal myocardial trabeculae morphology / MGI
  • abnormal cochlear ganglion morphology / MGI
  • abnormal neural crest cell migration / MGI
  • abnormal heart atrium morphology / MGI
  • dilated heart atrium / MGI
  • abnormal vitelline vasculature morphology / MGI
  • kinked neural tube / MGI
  • nervous system phenotype / MGI
  • abnormal ventral spinal root morphology / MGI
  • decreased Schwann cell precursor number / MGI
  • decreased neuronal precursor cell number / MGI
  • cardiovascular system phenotype / MGI
  • reproductive system phenotype / MGI
  • abnormal paravertebral ganglion morphology / MGI
  • abnormal atrium myocardium morphology / MGI
  • atrioventricular block / MGI
  • perinatal lethality, complete penetrance / MGI
  • embryonic lethality, complete penetrance / MGI
  • embryonic lethality during organogenesis, complete penetrance / MGI
  • abnormal phrenic nerve innervation pattern to diaphragm / 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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