- 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 |
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 |
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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