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Sox11tm1.2Vlf
Targeted Allele Detail
Summary
Symbol: Sox11tm1.2Vlf
Name: SRY (sex determining region Y)-box 11; targeted mutation 1.2, Veronique Lefebvre
MGI ID: MGI:5285292
Synonyms: Sox11tm2.2Weg
Gene: Sox11  Location: Chr12:27384263-27392573 bp, - strand  Genetic Position: Chr12, 9.95 cM, cytoband A3
Alliance: Sox11tm1.2Vlf page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:175338
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Cre-mediated recombination removed the coding region and neo cassette. (J:175338)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 9 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 Sox11 Mutation:  15 strains or lines available
References
Original:  J:175338 Bhattaram P, et al., Organogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitors. Nat Commun. 2010;1:9
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
10/29/2024
MGI 6.24
The Jackson Laboratory