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

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.

Strain of Origin:

CByJ.A-Atp2b2dfw-2J/J

Allele Type:    Spontaneous Mutation:    Undefined   Mutation details: A failed complementation test with Fgfr3tm1Dor demonstrated that this mutation is an allele of Fgfr3. (J:178517) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

2 anatomical structure(s)

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:	52 strains or lines available

Original:	J:178517 Harris BS, et al., A new spontaneous mutation in Fgfr3. MGI Direct Data Submission. 2011;
All:	1 reference(s)