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Sqstm1tm1.1Ewa
Targeted Allele Detail
Summary
Symbol: Sqstm1tm1.1Ewa
Name: sequestosome 1; targeted mutation 1.1, Eiji Warabi
MGI ID: MGI:5546006
Synonyms: p62flox
Gene: Sqstm1  Location: Chr11:50090193-50101654 bp, - strand  Genetic Position: Chr11, 30.36 cM, cytoband B1.2
Alliance: Sqstm1tm1.1Ewa page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:201732
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted upstream of exon 1 and a loxP site and FRT flanked selection cassette were inserted downstream of exon 1. The selection cassette was removed leaving exon 1 floxed. (J:201732)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
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 Sqstm1 Mutation:  35 strains or lines available
References
Original:  J:201732 Harada H, et al., Deficiency of p62/Sequestosome 1 causes hyperphagia due to leptin resistance in the brain. J Neurosci. 2013 Sep 11;33(37):14767-77
All:  11 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
10/29/2024
MGI 6.24
The Jackson Laboratory