About   Help   FAQ
Fgfr3m1J
Spontaneous Allele Detail
Summary
Symbol: Fgfr3m1J
Name: fibroblast growth factor receptor 3; mutation 1, Jackson
MGI ID: MGI:4847622
Gene: Fgfr3  Location: Chr5:33879068-33894412 bp, + strand  Genetic Position: Chr5, 17.83 cM, cytoband B
Alliance: Fgfr3m1J page
Abnormal spine curvature in Fgfr3m1J/Fgfr3m1J mice

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  CByJ.A-Atp2b2dfw-2J/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsA failed complementation test with Fgfr3tm1Dor demonstrated that this mutation is an allele of Fgfr3. (J:178517)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Fgfr3 Mutation:  54 strains or lines available
References
Original:  J:178517 Harris BS, et al., A new spontaneous mutation in Fgfr3. MGI Direct Data Submission. 2011;
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory