Conventional / global / constitutive KO
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Browse 1 Fgf9 mouse model including knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Fgf9, mouse ortholog of human FGF9, encodes a secreted ligand that homodimerizes through an N-terminal interface, which occludes part of its heparan sulfate binding surface and thereby extends diffusion range, and it activates FGFR2c, FGFR3c, and FGFR1c with ERK output. Its most decisive role is in gonadal sex determination, where it forms a feedforward loop with SOX9 that antagonizes WNT4 and RSPO1, such that XY nulls undergo male-to-female sex reversal, and it further drives lung mesenchymal proliferation, cerebellar and inner ear development, and intestinal mesenchyme growth. Germline deletion is lethal at birth from lung hypoplasia, so conditional floxed alleles are required for postnatal work, while human heterozygous missense variants that increase dimerization cause multiple synostoses syndrome 3 with elbow and knee fusion, making gain-of-function knockins the correct model for that disease class. Overlap with Fgf16 and Fgf20 at shared c-isoform receptors warrants compound alleles. Match allele to gonadal fate, alveolarization, or joint fusion endpoints.
ingenious targeting laboratory offers 1 distinct Fgf9 (FGF9) catalog mouse model in the FGF family, featuring conditional knockout and standard knockout. Researchers can order pre-developed catalog lines or request a custom mouse model, including humanized, knockin, and transgenic variations with verified germline transmission.
| Model Availability | Allele Class Options |
|---|---|
| 1 Ready Catalog Line | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) |
| Advanced Modifications | Humanized, Knockin, Transgenic |
Knockout
Conditional knockout
Knockin
Humanized
Transgenic / overexpression
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Knockout, conditional, knockin, humanized, and related paths for Fgf9 (human FGF9). Catalog lines ship when inventory exists. Everything else is a generation quote.
Specify tissue or Cre driver on quote
Convertible floxed allele pathway
Multi allele / compound knockout project
BAC scale deletion or targeting
LSL or conditional expression knockin
Domain or partial humanization scope
Checkpoint IO humanization when gene is a checkpoint target
Multi humanized / combination IO project
BAC transgenic or large fragment insert
Tamoxifen or dox inducible Cre
Dual recombinase breeding scheme
Flp or FRT derivative allele pairing
Catalog reporter lines not tied to a single gene allele
Specify rat on quote
Specify rabbit on quote
Background substrain on quote
Background strain on quote
1 Fgf9 line with QC documentation and technical support.
Fgf9-KO
KOKO
The exon2 of Fgf9 gene was deleted to generate Fgf9 knockout mouse.
We have 1 Fgf9 model available — including Knockout types. Contact us today for current availability and our fastest turnaround options. All models come with full QC documentation and technical support.
Best pricing in the industry. Get a quote in 24 hours. Our team of PhD scientists is available to help you select the right model for your research.
Order catalog modelA Fgf9 knockout mouse has the Fgf9 gene permanently inactivated, enabling loss of function studies.
Jump to catalog backed pages for Fgf9 organized by modification type. Each URL is indexable and matches common search patterns.
Send the Fgf9 line to a U.S. barrier facility for colony maintenance, cohort production, and complex breeding schemes through mouse breeding services.