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Pnntm1Sps
Targeted Allele Detail
Summary
Symbol: Pnntm1Sps
Name: pinin; targeted mutation 1, Stephen P Sugrue
MGI ID: MGI:4455340
Synonyms: Pnn3f, Pnnneo-flox
Gene: Pnn  Location: Chr12:59113705-59120803 bp, + strand  Genetic Position: Chr12, 26.0 cM
Alliance: Pnntm1Sps 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, Hypomorph)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted in intron 2 and a floxed neo cassette was inserted in intron 8 via homologous recombination. Western blot analysis indicates a reduction in protein expression in homozygous and heterozygous mice, thus, this is a hypomorphic allele. (J:123288)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 9 assay results
In Structures Affected by this Mutation: 10 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:  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
10/29/2024
MGI 6.24
The Jackson Laboratory