- increased mean platelet volume / IMPC
- abnormal spleen morphology / IMPC
- increased circulating creatine kinase level / IMPC
- vertebral fusion / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased hematocrit / IMPC
- abnormal cornea morphology / IMPC
- abnormal coat/hair pigmentation / IMPC
- increased circulating alanine transaminase level / IMPC
- increased grip strength / IMPC
- abnormal snout morphology / IMPC
- abnormal cranium morphology / IMPC
- fused cornea and lens / IMPC
- abnormal thymus morphology / IMPC
- abnormal head morphology / IMPC
- abnormal spine curvature / IMPC
- abnormal eye morphology / IMPC
- enlarged thymus / IMPC
- abnormal heart morphology / IMPC
- increased circulating lactate dehydrogenase level / IMPC
- microphthalmia / IMPC
- anophthalmia / IMPC
- decreased spleen weight / IMPC
- corneal opacity / IMPC
- abnormal skin morphology / IMPC
- enlarged heart / IMPC
- increased circulating phosphate level / IMPC
- increased eosinophil cell number / IMPC
- decreased body weight / IMPC
- decreased hemoglobin content / IMPC
- narrow eye opening / IMPC
- decreased erythrocyte cell number / IMPC
B6NCrl;B6N-Atm1Brd Rnf168tm2a(EUCOMM)Hmgu/Ph
Status | Available to order |
EMMA ID | EM:12637 |
Citation information | RRID:IMSR_EM:12637 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 | B6NCrl;B6N-Atm1Brd Rnf168tm2a(EUCOMM)Hmgu/Ph |
Alternative name | HEPD0798_7_B10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Rnf168tm2a(EUCOMM)Hmgu |
Gene/Transgene symbol | Rnf168 |
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 | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0798_7_B10. 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 | Institute of Molecular Genetics, Prague, Czech Republic |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- RIDDLE syndrome / Orphanet_420741
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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