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Usp49em1Gpt
Endonuclease-mediated Allele Detail
Summary
Symbol: Usp49em1Gpt
Name: ubiquitin specific peptidase 49; endonuclease-mediated mutation 1, GemPharmatech Co., Ltd
MGI ID: MGI:6403288
Synonyms: Usp49-, Usp49em1Cd182, Usp49em1Nju
Gene: Usp49  Location: Chr17:47941615-47997663 bp, + strand  Genetic Position: Chr17, 23.72 cM
Alliance: Usp49em1Gpt page
Mutation
origin
Strain of Origin:  C57BL/6NGpt
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExon 3 was targeted using two gRNAs (AGACCACATGACTCGGAAGAGGG and AGCCACGGAAGGCGGGAATCAGG) and CRISPR/Cas9 technology, resulting in a 182 bp deletion. This causes a frameshift and premature stop codon. (J:285681)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Usp49 Mutation:  52 strains or lines available
References
Original:  J:285681 Ye L, et al., USP49 negatively regulates cellular antiviral responses via deconjugating K63-linked ubiquitination of MITA. PLoS Pathog. 2019 Apr;15(4):e1007680
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
04/16/2024
MGI 6.23
The Jackson Laboratory