C57Bl/6NTac-Aqp5em1(IMPC)H/H
| Status | Available to order |
| EMMA ID | EM:16754 |
| Citation information | RRID:IMSR_EM:16754 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/6NTac-Aqp5em1(IMPC)H/H |
| Alternative name | C57Bl/6NTac-Aqp5 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Aqp5em1(IMPC)H |
| Gene/Transgene symbol | Aqp5 |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This strain carries a CRISPR/Cas9 induced deletion of 606 nt from Aqp5 gene, across two critical exons (ENSMUSE00000297625 & ENSMUSE00001018343.) to introduce a frameshift resulting in a premature stop codon null allele in 3 of 4 transcripts. |
| Phenotypic information | Homozygous:These mice are part of the International Mouse Phenotyping Consortium (IMPC) and will be phenotyped through a standardised phenotyping pipeline. Details of the pipeline and data, when available, can be viewed at https://www.mousephenotype.org/data/genes/MGI:106215Heterozygous:These mice are part of the International Mouse Phenotyping Consortium (IMPC) and will be phenotyped through a standardised phenotyping pipeline. Details of the pipeline and data, when available, can be viewed at https://www.mousephenotype.org/data/genes/MGI:106215 |
| Breeding history | Coisogenic on maintained background |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Non-epidermolytic palmoplantar keratoderma / Orphanet_2337
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