- abnormal coat/hair pigmentation / IMPC
C57BL/6N-Psg26em1(IMPC)Wtsi/WtsiPh
Status | Available to order |
EMMA ID | EM:13921 |
Citation information | RRID:IMSR_EM:13921 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-Psg26em1(IMPC)Wtsi/WtsiPh |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Psg26em1(IMPC)Wtsi |
Gene/Transgene symbol | Psg26 |
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 | Institute of Molecular Genetics, Prague, Czech Republic |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal coat/hair pigmentation / IMPC
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