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Hgstm2Tkh
Targeted Allele Detail
Summary
Symbol: Hgstm2Tkh
Name: HGF-regulated tyrosine kinase substrate; targeted mutation 2, Nobuyuki Tanaka
MGI ID: MGI:3818694
Synonyms: hrsloxP
Gene: Hgs  Location: Chr11:120358461-120374805 bp, + strand  Genetic Position: Chr11, 84.16 cM
Alliance: Hgstm2Tkh page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:141391
Parent Cell Line:  TT2 (ES Cell)
Strain of Origin:  (C57BL/6NCrlj x CBA/JNCrlj)F1
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted upstream of exon 2 and an frt-flanked neo cassette with a 3' loxP site was inserted downstream of exon 4. Germ line, flp-mediated recombination was used to remove the neo cassette leaving exons 2 through 4 floxed. (J:141391)
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 Hgs Mutation:  40 strains or lines available
References
Original:  J:141391 Tamai K, et al., Loss of hrs in the central nervous system causes accumulation of ubiquitinated proteins and neurodegeneration. Am J Pathol. 2008 Dec;173(6):1806-17
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