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Pcdh15tm1.1Ugds
Targeted Allele Detail
Summary
Symbol: Pcdh15tm1.1Ugds
Name: protocadherin 15; targeted mutation 1.1, Unite de Genetique des Deficits Sensoriels
MGI ID: MGI:5566900
Synonyms: Pcdh15 ex38-fl1.1UGDS
Gene: Pcdh15  Location: Chr10:72935174-74485569 bp, + strand  Genetic Position: Chr10, 37.43 cM
Alliance: Pcdh15tm1.1Ugds page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:209275
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S1/SvImJ
Mutation
description
Allele Type:    Targeted (Conditional ready)
Mutation:    Insertion
    Exon 38 was floxed. Flp-mediated recombination removed the neomycin selection cassette. (J:209275)
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 Pcdh15 Mutation:  135 strains or lines available
References
Original:  J:209275 Petit C, Direct Data Submission for Pcdh15 floxed allele from Ugds. MGI Direct Data Submission. 2014;
All:  4 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