BALB/cN-Nxnl1tm1.1Ics/Ics
| Status | Available to order |
| EMMA ID | EM:16222 |
| Citation information | RRID:IMSR_EM:16222 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 | BALB/cN-Nxnl1tm1.1Ics/Ics |
| Alternative name | Nxnl1tm1.1/Ics |
| Strain type | Targeted Mutant Strains : Point mutation |
| Allele/Transgene symbol | Nxnl1tm1.1Ics |
| Gene/Transgene symbol | Nxnl1 |
Information from provider
| Provider | Thierry Léveillard |
| Provider affiliation | Institut de la Vision, INSERM UMR_S 968, CNRS UMR_7210, Sorbonne Université |
| Genetic information | A floxed auto-excisable selection cassette (neoR-protamine cre) was inserted upstream exon 2 (ENSMUSE00000914521, Nxnl1-201 GRCm39); glutamine codon 114 (CAG) in exon 2 was changed to a premature STOP codon (TAG; c.340C>T p.Q>*). |
| Phenotypic information | Homozygous:N/AHeterozygous:N/A |
| Breeding history | 100% BALB/cNCrl |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
MGI phenotypes (gene matching)
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