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Rnf168Gt(405F11)Cmhd
Gene trapped Allele Detail
Nomenclature
Symbol: Rnf168Gt(405F11)Cmhd
Name: ring finger protein 168; gene trap 405F11, Centre for Modeling Human Disease
MGI ID: MGI:4962718
Gene: Rnf168  Location: Chr16:32096277-32120252 bp, + strand  Genetic Position: Chr16, 22.51 cM, cytoband B2
Mutation
origin
Mutant Cell Line:  405F11
Germline Transmission:  Earliest citation of germline transmission: J:198260
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Gene trapped (Null/knockout, Reporter)
Mutation:    Insertion of gene trap vector     Vector: GepNMDi3
 
Mutation detailsThe gene trap vector inserted upstream of exon 6. Western blot analysis confirmed the absence of protein expression in the mouse embryonic fibroblasts and splenocytes. (J:198260)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 3 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Rnf168 Mutation:  68 strains or lines available
References
Original:  J:141210 Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI), Mouse Gene Trap Data Load from dbGSS. Database Download. 2008;
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
08/03/2022
MGI 6.21
The Jackson Laboratory