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Fgfr1tm1.1Upir
Targeted Allele Detail
Summary
Symbol: Fgfr1tm1.1Upir
Name: fibroblast growth factor receptor 1; targeted mutation 1.1, Ulla Pirvola
MGI ID: MGI:3529270
Synonyms: Fgfr1deltaflox
Gene: Fgfr1  Location: Chr8:26008808-26067819 bp, + strand  Genetic Position: Chr8, 14.12 cM
Alliance: Fgfr1tm1.1Upir page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:78879
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThis allele was generated through cre mediated recombination of Fgfr1tm1Upir resulting in deletion of exons 8-15. (J:78879)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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 Fgfr1 Mutation:  223 strains or lines available
References
Original:  J:78879 Pirvola U, et al., FGFR1 is required for the development of the auditory sensory epithelium. Neuron. 2002 Aug 15;35(4):671-80
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
10/22/2024
MGI 6.24
The Jackson Laboratory