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Uhrf1MommeD40
Chemically induced Allele Detail
Summary
Symbol: Uhrf1MommeD40
Name: ubiquitin-like, containing PHD and RING finger domains, 1; modifier of murine metastable epialleles, D40
MGI ID: MGI:5515394
Gene: Uhrf1  Location: Chr17:56610405-56630486 bp, + strand  Genetic Position: Chr17, 29.26 cM, cytoband D-E1
Alliance: Uhrf1MommeD40 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsA T-to-A single point mutation in exon 17 is predicted to result in a Y778 to a stop codon in the encoded protein. The encoded protein was not detected on Western blot of embryonic tissue, suggesting that this allele is null. (J:201508)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Uhrf1 Mutation:  53 strains or lines available
References
Original:  J:201508 Daxinger L, et al., An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse. Genome Biol. 2013 Sep 11;14(9):R96
All:  1 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
12/30/2025
MGI 6.24
The Jackson Laboratory