BALB/c-Ceacam16tm1Wzm/Ieg

Status

Available to order

EMMA IDEM:06746
International strain nameBALB/c-Ceacam16tm1Wzm/Ieg
Alternative nameCeacam16tm1Wzm
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolCeacam16tm1Wzm
Gene/Transgene symbolCeacam16

Information from provider

ProviderWolfgang Zimmermann
Provider affiliationTumor Immunology Laboratory, LIFE Center, University Hospital, Ludwig-Maximilians University Muenchen
Additional owner
Genetic informationCeacam16tm1Wzm mice lack a 6.8-kb region in the Ceacam16 gene that comprises exons 2-4 and part of exon 5 that was replaced by a 1.7-kb neo cassette.
Phenotypic informationIn Ceacam16tm1Wzm mice the hearing threshold for frequencies below 10 kHz and above 22 kHz is raised.
Breeding historyAn ES cell clone was injected into C57BL/6J blastocysts, and these were implanted into a NMRI foster mother. The resulting male chimeras were backcrossed to BALB/c females to identify germ line transmission of the targeted allele and to produce mice heterozygous for the null mutation. F1 intercrosses of heterozygous mice resulted in F2 offspring on pure BALB/c (Charles River) background.
References
  • Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.;Kammerer Robert, Rüttiger Lukas, Riesenberg Rainer, Schäuble Constanze, Krupar Rosemarie, Kamp Annegret, Sunami Kishiko, Eisenried Andreas, Hennenberg Martin, Grunert Fritz, Bress Andreas, Battaglia Sebastiano, Schrewe Heinrich, Knipper Marlies, Schneider Marlon R, Zimmermann Wolfgang, ;2012;The Journal of biological chemistry;287;21584-98; 22544735
Homozygous fertileyes
Homozygous viableyes
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreHelmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany
Animals used for archivinghomozygous BALB/c, wild-type BALB/c
Stage of embryos2-cell

Disease and phenotype information

MGI allele-associated human disease models

Orphanet associated rare diseases, based on orthologous gene matching

    • Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
    • Autosomal dominant non-syndromic sensorineural deafness type DFNA / Orphanet_90635
IMPC phenotypes (gene matching)
  • increased circulating sodium level / IMPC
  • sclerocornea / IMPC
  • decreased circulating free fatty acids level / IMPC
MGI phenotypes (allele matching)
  • abnormal distortion product otoacoustic emission / MGI
  • nonsyndromic hearing loss / MGI
  • increased or absent threshold for auditory brainstem response / MGI
MGI phenotypes (gene matching)
  • abnormal distortion product otoacoustic emission / MGI
  • nonsyndromic hearing loss / MGI
  • abnormal otoacoustic response / MGI
  • increased or absent threshold for auditory brainstem response / MGI
  • absent Hensen stripe / MGI
  • abnormal tectorial membrane striated-sheet matrix morphology / MGI

Literature references

  • Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.;Kammerer Robert, Rüttiger Lukas, Riesenberg Rainer, Schäuble Constanze, Krupar Rosemarie, Kamp Annegret, Sunami Kishiko, Eisenried Andreas, Hennenberg Martin, Grunert Fritz, Bress Andreas, Battaglia Sebastiano, Schrewe Heinrich, Knipper Marlies, Schneider Marlon R, Zimmermann Wolfgang, ;2012;The Journal of biological chemistry;287;21584-98; 22544735

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 embryos. Delivered in 4 weeks (after paperwork in place). €1740*
  • 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)
For this strain no provider MTA is needed. Distribution is based on the EMMA conditions only.

EMMA conditions
Legally binding conditions for the transfer

Other EMMA strains

Not found what you were looking for? Search here for other strains available from EMMA.


Search
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).