- abnormal ear position / IMPC
- increased circulating amylase level / IMPC
- increased circulating calcium level / IMPC
- absent pinna reflex / IMPC
- increased blood urea nitrogen level / IMPC
- increased circulating HDL cholesterol level / IMPC
- decreased circulating chloride level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating total protein level / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating creatinine level / IMPC
C57BL/6N-Lrbatm1.1Ics/Ics
| Status | Available to order |
| EMMA ID | EM:16217 |
| Citation information | RRID:IMSR_EM:16217 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-Lrbatm1.1Ics/Ics |
| Alternative name | Lrbatm1.1Ics/Ics |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Lrbatm1.1Ics |
| Gene/Transgene symbol | Lrba |
Information from provider
| Provider | Frédéric Rieux-laucat |
| Provider affiliation | Institut Imagine |
| Genetic information | A loxP site was inserted into intron 1 and an FRT site-flanked neomycin resistance gene cassette was inserted into intron 2. Subsequent flp-mediated recombination led to a conditional-ready allele with floxed exon 2 (ENSMUSE00000331229; GRCm39, Lrba-201). |
| Phenotypic information | Homozygous:N/AHeterozygous:N/A |
| Breeding history | 100% C57BL/6N (C57BL/6NCrl 99,90% C57BL/6NTac 0,10%) |
| 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
Orphanet associated rare diseases, based on orthologous gene matching
- Combined immunodeficiency due to LRBA deficiency / Orphanet_445018
IMPC phenotypes (gene matching)
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