- abnormal thymus morphology / IMPC
- abnormal vertebrae morphology / IMPC
- abnormal testis morphology / IMPC
- abnormal vertebral arch morphology / IMPC
- hydrometra / IMPC
- abnormal heart left ventricle morphology / IMPC
- enlarged thymus / IMPC
- small testis / IMPC
- abnormal heart morphology / IMPC
- enlarged heart / IMPC
- abnormal spleen morphology / IMPC
- small spleen / IMPC
- enlarged spleen / IMPC
- increased cardiac muscle contractility / IMPC
- kyphosis / IMPC
- abnormal retina morphology / IMPC
- abnormal spine curvature / IMPC
- abnormal uterus morphology / IMPC
B6.129-Calb1tm1Mpin/JBiat
Status | Available to order |
EMMA ID | EM:09881 |
Citation information | RRID:IMSR_EM:09881 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 | B6.129-Calb1tm1Mpin/JBiat |
Alternative name | B6.129-Calb1tm1Mpin |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Calb1tm1Mpin |
Gene/Transgene symbol | Calb1 |
Information from provider
Provider | Michael Meyer |
Provider affiliation | Department of Cellular Physiology, LMU München |
Genetic information | Targeted Mutation (replacement of exon 1 of the Calbindin D28k gene by a targeting vector (PGK-promoter, neo-cassette). |
Phenotypic information | Homozygous:Mice homozygous for the Calb1 targeted mutation are viable and fertile. They show severe impairment in tests of motor coordination and exhibit ataxia when challenged on a runway. These results suggest functional deficits in cerebellar pathways. Confocal calcium imaging of cerebellar Purkinje cells reveals marked changes of synaptically-evoked postsynaptic calcium transients. No overt phenotype in normal cage environment.Heterozygous:not known (no overt phenotype in normal cage environment) |
Breeding history | History before 2000 not known; since 2000 backcrossing to C57BL/6J, since 2011 to C57BL/6N. |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | University of Veterinary Medicine, Vienna, Austria |
Animals used for archiving | homozygous C57BL/6N males |
Disease and phenotype information
IMPC phenotypes (gene matching)
Literature references
- Ataxia and altered dendritic calcium signaling in mice carrying a targeted null mutation of the calbindin D28k gene.;Airaksinen M S, Eilers J, Garaschuk O, Thoenen H, Konnerth A, Meyer M, ;1997;Proceedings of the National Academy of Sciences of the United States of America;94;1488-93; 9037080
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