- increased circulating alkaline phosphatase level / IMPC
- abnormal retina morphology / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- increased circulating lipase level / IMPC
- abnormal lens morphology / IMPC
- abnormal tail morphology / IMPC
- abnormal tail length / IMPC
- decreased total retina thickness / IMPC
- abnormal optic disk morphology / IMPC
- increased startle reflex / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal retina vasculature morphology / IMPC
- increased circulating amylase level / IMPC
C57BL/6N-Cant1tm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:08006 |
Citation information | RRID:IMSR_EM:08006 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-Cant1tm1a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0624_1_E03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cant1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cant1 |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0624_1_E03. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTac (USA) males, wild-type C57BL/6NTac (USA) females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Desbuquois syndrome / Orphanet_1425
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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