- decreased bone mineral content / IMPC
- decreased circulating total protein level / IMPC
- abnormal coat/hair pigmentation / IMPC
- abnormal bone structure / IMPC
- increased total body fat amount / IMPC
- decreased lean body mass / IMPC
- abnormal vocalization / IMPC
- decreased bone mineral density / IMPC
- increased circulating triglyceride level / IMPC
- decreased heart weight / IMPC
C57BL/6N-Rab28em2(IMPC)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:13797 |
Citation information | RRID:IMSR_EM:13797 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-Rab28em2(IMPC)Wtsi/WtsiOrl |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Rab28em2(IMPC)Wtsi |
Gene/Transgene symbol | Rab28 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Cone rod dystrophy / Orphanet_1872
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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