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Dnmt3bMommeD14
Chemically induced Allele Detail
Summary
Symbol: Dnmt3bMommeD14
Name: DNA methyltransferase 3B; modifier of murine metastable epialleles, D14
MGI ID: MGI:5515362
Synonyms: MommeD14
Gene: Dnmt3b  Location: Chr2:153491370-153529650 bp, + strand  Genetic Position: Chr2, 75.79 cM, cytoband A2-A3
Alliance: Dnmt3bMommeD14 page
Mutation
origin
Strain of Origin:  FVB/NJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA T-to-C single point mutation at the 5' splice site of intron 13 is predicted to result in a splicing defect in the mRNA. qRT-PCR and Western analyses showed that the mRNA and protein levels were not grossly affected, suggesting that this allele is a hypomorph. (J:198944, J:201508)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
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 Dnmt3b Mutation:  52 strains or lines available
References
Original:  J:198944 Youngson NA, et al., No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generations. Mamm Genome. 2013 Jun;24(5-6):206-17
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory