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Sox17tm3.1Heli
Targeted Allele Detail
Summary
Symbol: Sox17tm3.1Heli
Name: SRY (sex determining region Y)-box 17; targeted mutation 3.1, Heiko Lickert
MGI ID: MGI:5428890
Synonyms: Sox17SCF
Gene: Sox17  Location: Chr1:4561154-4567577 bp, - strand  Genetic Position: Chr1, 1.65 cM
Alliance: Sox17tm3.1Heli page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:185482
Parent Cell Line:  IDG3.2 (ES Cell)
Strain of Origin:  (C57BL/6J x 129S6/SvEvTac)F1
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Insertion
 
Mutation detailsThe translational stop codon in exon 5 was replaced with an in-frame open reading frame of mCherry followed by a floxed PGK-neo cassette. Cre mediated recombination removed the neo cassette. Expression and localization of the fusion protein recapitulates endogenous gene expression and localization. (J:185482)
Generation of the Sox17tm3.1Heli allele
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 Sox17 Mutation:  28 strains or lines available
References
Original:  J:185482 Burtscher I, et al., The Sox17-mCherry fusion mouse line allows visualization of endoderm and vascular endothelial development. Genesis. 2012 Jun;50(6):496-505
All:  4 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