C57BL/6N-Krt5em1(IMPC)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:13823 |
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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