Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

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

Germline Transmission:	Earliest citation of germline transmission: J:78879
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion   Mutation details: This allele was generated through cre mediated recombination of Fgfr1tm1Upir resulting in deletion of exons 8-15. (J:78879)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

10 anatomical structure(s)

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:	221 strains or lines available

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)