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Pnntm1.1Sps
Targeted Allele Detail
Summary
Symbol: Pnntm1.1Sps
Name: pinin; targeted mutation 1.1, Stephen P Sugrue
MGI ID: MGI:4455341
Synonyms: Pnn2f, Pnnflox
Gene: Pnn  Location: Chr12:59113705-59120803 bp, + strand  Genetic Position: Chr12, 26.0 cM
Alliance: Pnntm1.1Sps page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:123288
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted in intron 2 and a floxed neo cassette was inserted in intron 8 via homologous recombination. Cre mediated recombination removed the neo cassette leaving exons 3 - 8 floxed. (J:123288)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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 Pnn Mutation:  31 strains or lines available
References
Original:  J:123288 Joo JH, et al., Role of Pinin in neural crest, dorsal dermis, and axial skeleton development and its involvement in the regulation of Tcf/Lef activity in mice. Dev Dyn. 2007 Aug;236(8):2147-58
All:  5 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
11/05/2024
MGI 6.24
The Jackson Laboratory