- decreased bone mineral density / IMPC
- abnormal retina morphology / IMPC
- decreased locomotor activity / IMPC
- decreased startle reflex / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
- abnormal auditory brainstem response / IMPC
- decreased lymphocyte cell number / IMPC
- decreased blood urea nitrogen level / IMPC
- increased prepulse inhibition / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased total retina thickness / IMPC
- decreased large unstained cell number / IMPC
C57BL/6N-Dyrk1btm1b(EUCOMM)Wtsi/Ics
| Status | Under development - register interest |
| EMMA ID | EM:16686 |
| Citation information | RRID:IMSR_EM:16686 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 | C57BL/6N-Dyrk1btm1b(EUCOMM)Wtsi/Ics |
| Alternative name | EPD0775_3_H05 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Dyrk1btm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Dyrk1b |
| Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | This mouse line originates from EUCOMM ES clone EPD0775_3_H05. 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 (Gt(ROSA)26Sortm1(ACTB-cre,-EGFP)Ics). Click here for more information on EUCOMM final vectors. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal auditory brainstem response / IMPC
- decreased blood urea nitrogen level / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
- decreased total retina thickness / IMPC
- decreased bone mineral density / IMPC
- decreased large unstained cell number / IMPC
- increased prepulse inhibition / IMPC
- decreased locomotor activity / IMPC
- abnormal retina morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased lymphocyte cell number / IMPC
- decreased startle reflex / IMPC
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