- 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 |
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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