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Sox4tm1.1Vlf
Targeted Allele Detail
Summary
Symbol: Sox4tm1.1Vlf
Name: SRY (sex determining region Y)-box 4; targeted mutation 1.1, Veronique Lefebvre
MGI ID: MGI:3773013
Synonyms: Sox4fl-
Gene: Sox4  Location: Chr13:29132902-29137682 bp, - strand  Genetic Position: Chr13, 12.87 cM, cytoband A3-A5
Alliance: Sox4tm1.1Vlf page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:130461
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThe coding region of the gene was removed by germ-line, cre-mediated recombination. The absence of absence of transcript was confirmed by northern blot analysis on total RNA from E12.5 embryos. (J:130461)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 2 assay results
In Structures Affected by this Mutation: 4 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 Sox4 Mutation:  23 strains or lines available
References
Original:  J:130461 Penzo-Mendez A, et al., Generation of mice harboring a Sox4 conditional null allele. Genesis. 2007 Dec;45(12):776-80
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
10/22/2024
MGI 6.24
The Jackson Laboratory