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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
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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)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory