- dry eyes / MGI
- postnatal lethality / MGI
- abnormal external female genitalia morphology / MGI
- clitoris hypoplasia / MGI
- keratoconjunctivitis sicca / MGI
- circling / MGI
- hyperactivity / MGI
- head bobbing / MGI
- abnormal superior semicircular canal morphology / MGI
- absent lateral semicircular canal / MGI
- decreased lateral semicircular canal size / MGI
- increased cochlear inner hair cell number / MGI
- increased cochlear outer hair cell number / MGI
- abnormal round window morphology / MGI
- abnormal stapes morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- skeleton phenotype / MGI
C3HeB/FeJ-Crsl/IegWtsiCnbc
Status | Available to order |
EMMA ID | EM:04919 |
Citation information | RRID:IMSR_EM:04919 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 name | C3HeB/FeJ-Crsl/IegWtsiCnbc |
Alternative name | Carousel |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Crsl |
Gene/Transgene symbol | Crsl |
Information from provider
Provider | Karen Steel |
Provider affiliation | Wellcome Trust Sanger Institute |
Additional owner | Prof. M. Hrabé de Angelis, Helmholtz Zentrum München, Neuherberg, Germany |
Genetic information | ENU-induced mutation at proximal chromosome 4. |
Phenotypic information | Circling, head-bobbing and hyperactive mutant, maps to proximal chromosome 4. Phenotype indistinguishable from Chd7 mutations. |
Breeding history | Originated from ENU mutagenesis programme in Munich, Helmholtz Centrum, on a C3HeB/FeJ background and bred on the same background within a closed colony or backcrossed to C3HeB/FeJ ever since. |
References |
|
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- dry eyes / MGI
- circling / MGI
- hyperactivity / MGI
- head bobbing / MGI
- postnatal lethality / MGI
- abnormal superior semicircular canal morphology / MGI
- abnormal external female genitalia morphology / MGI
- absent lateral semicircular canal / MGI
- decreased lateral semicircular canal size / MGI
- increased cochlear inner hair cell number / MGI
- increased cochlear outer hair cell number / MGI
- abnormal round window morphology / MGI
- abnormal stapes morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- skeleton phenotype / MGI
- clitoris hypoplasia / MGI
- keratoconjunctivitis sicca / MGI
Literature references
- Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4.;Hawker Kelvin, Fuchs Helmut, Angelis Martin Hrabéde, Steel Karen P, ;2005;International journal of audiology;44;171-7; 15916118
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).