C57BL/6J-Pcdh19em2H/H
| Status | Available to order |
| EMMA ID | EM:15699 |
| Citation information | RRID:IMSR_EM:15699 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/6J-Pcdh19em2H/H |
| Alternative name | C57BL/6J-Pcdh19 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Pcdh19em2H |
| Gene/Transgene symbol | Pcdh19 |
Information from provider
| Provider | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | As reported by Mouse Genome Informatics, Pcdh19, a protein coding gene, codes for protocadherin-19 and is associated with developmental and epileptic encephalopathy in Humans. This line was generated by introducing a Knock-in of ddCre into the 5' UTR of Pcdh19 made by CRISPR/Cas9 gene editing. The knock-in was introduced via pronuclear injection into 1-cell stage embryo. |
| Phenotypic information | Homozygous:To be determinedHeterozygous:To be determined |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |