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Cdx2tm2.1Fbe
Targeted Allele Detail
Summary
Symbol: Cdx2tm2.1Fbe
Name: caudal type homeobox 2; targeted mutation 2.1, F Beck
MGI ID: MGI:5308967
Synonyms: Cdx2ko
Gene: Cdx2  Location: Chr5:147237710-147244059 bp, - strand  Genetic Position: Chr5, 86.86 cM, cytoband G2-G3
Alliance: Cdx2tm2.1Fbe page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:179732
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Exon 2 was floxed via homologous recombination and then deleted via cre mediated recombination. (J:179732)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Cdx2 Mutation:  22 strains or lines available
References
Original:  J:179732 Stringer EJ, et al., Cdx2 determines the fate of postnatal intestinal endoderm. Development. 2012 Feb;139(3):465-74
All:  1 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