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

Symbol:	Fgf9tm1Dor
Name:	fibroblast growth factor 9; targeted mutation 1, David Ornitz
MGI ID:	MGI:2135961
Synonyms:	Fgf9-
Gene:	Fgf9  Location: Chr14:58308004-58350177 bp, + strand  Genetic Position: Chr14, 30.51 cM, cytoband D
Alliance:	Fgf9tm1Dor page

Germline Transmission:	Earliest citation of germline transmission: J:68379
Parent Cell Line:	SM1 (ES Cell)
Strain of Origin:	129S6/SvEvTac

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: Replacement of 500 bp of genomic sequence with a neomycin resistance cassette, resulting in a deletion eliminating 224 bp of the 277 bp in the protein-coding region of exon 1 and extending into the first intron. (J:68379) Inheritance:    Recessive

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

In Mice Carrying this Mutation:	46 assay results
In Structures Affected by this Mutation:	15 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 Fgf9 Mutation:	15 strains or lines available

Original:	J:68379 Colvin JS, et al., Male-to-female sex reversal in mice lacking fibroblast growth factor 9. Cell. 2001 Mar 23;104(6):875-89
All:	37 reference(s)