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TasorMommeD20
Chemically induced Allele Detail
Summary
Symbol: TasorMommeD20
Name: transcription activation suppressor; modifier of murine metastable epialleles, D20
MGI ID: MGI:5659903
Gene: Tasor  Location: Chr14:27150791-27205512 bp, + strand  Genetic Position: Chr14, 16.51 cM, cytoband B
Alliance: TasorMommeD20 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsMice carrying Tg(Hba1-Gfp)1Ew were treated with ENU. A single base pair, T to C mutation, was detected in intron 1 at the a canonical splice site for exon 1/intron 1. Both the wild-type and a higher molecular weight mutant PCR product are detected in heterozygous mice. The aberrant splice product results in the incorporation of an additional 1,160 nucleotides. The resulting protein is predicted to incorporate 79 additional amino acids followed by a premature stop codon and be subject to nonsense mediated decay. Western blot analysis of testis lysates from heterozygous mice revealed reduced protein expression. (J:99816, J:216844)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Tasor Mutation:  93 strains or lines available
References
Original:  J:216844 Harten SK, et al., The first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development. Mamm Genome. 2014 Aug;25(7-8):293-303
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
04/23/2024
MGI 6.23
The Jackson Laboratory