C57BL/6N-Krt5em1(IMPC)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:13823 |
Citation information | RRID:IMSR_EM:13823 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-Krt5em1(IMPC)Wtsi/WtsiOulu |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Krt5em1(IMPC)Wtsi |
Gene/Transgene symbol | Krt5 |
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 | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Dowling-Degos disease / Orphanet_79145
- Epidermolysis bullosa simplex, generalized intermediate / Orphanet_79399
- Epidermolysis bullosa simplex, generalized severe / Orphanet_79396
- Epidermolysis bullosa simplex with mottled pigmentation / Orphanet_79397
- Epidermolysis bullosa simplex with circinate migratory erythema / Orphanet_158681
- Localized epidermolysis bullosa simplex / Orphanet_79400
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal esophageal epithelium morphology / MGI
- abnormal stomach morphology / MGI
- abnormal autopod morphology / MGI
- abnormal tongue epithelium morphology / MGI
- abnormal epidermal layer morphology / MGI
- abnormal tail morphology / MGI
- abnormal palate morphology / MGI
- absent gastric milk in neonates / MGI
- neonatal lethality, complete penetrance / MGI
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