- abnormal retina morphology / IMPC
C57BL/6N-Atm1Brd Irf7tm1(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:14100 |
Citation information | RRID:IMSR_EM:14100 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-Atm1Brd Irf7tm1(KOMP)Wtsi/WtsiOrl |
Alternative name | EPD0376_1_C05 |
Strain type | |
Allele/Transgene symbol | Irf7tm1(KOMP)Wtsi |
Gene/Transgene symbol | Irf7 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0376_1_C05. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal retina morphology / IMPC
MGI phenotypes (gene matching)
- increased susceptibility to viral infection / MGI
- abnormal T cell physiology / MGI
- decreased interferon-alpha secretion / MGI
- decreased interferon-beta secretion / MGI
- decreased circulating interferon-beta level / MGI
- abnormal interferon level / MGI
- increased susceptibility to viral infection induced morbidity/mortality / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).