- abnormal retina morphology / IMPC
C57BL/6N-Atm1Brd Irf7tm1(KOMP)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:14100 |
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:
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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
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