Conventional / global / constitutive KO
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Browse 2 Fzd2 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as Fzd2 conditional knockout mouse, Fzd2 knockout mouse. Contact us for availability and fast turnaround.
Fzd2, mouse ortholog of human FZD2, encodes a class F seven transmembrane receptor closely related to FZD1 and FZD7, binding Wnt ligands through its cysteine rich domain and coupling to both canonical beta-catenin signaling via LRP5 and LRP6 and to planar cell polarity signaling through Dishevelled, DAAM1 and RHOA with ROCK and JNK output. Heterozygous truncating variants near the C-terminal KTXXXW and PDZ binding region cause autosomal dominant Robinow syndrome and omodysplasia, and these act as dominant alleles rather than simple loss of function, which means a conventional null will not reproduce the human disease and a targeted truncation knockin is required. FZD2 is also induced during epithelial to mesenchymal transition and supports STAT3 dependent invasion in carcinoma. Single nulls are viable with cleft palate at low penetrance, but combined Fzd1 and Fzd2 deletion produces highly penetrant palatal clefting, confirming real redundancy. Match design to question, using truncation knockins for skeletal dysplasia and compound conditional alleles for developmental requirement.
ingenious targeting laboratory offers 2 distinct Fzd2 (FZD2) catalog mouse models, 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 |
|---|---|
| 2 Ready Catalog Lines | 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 Fzd2 (human FZD2). 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
2 Fzd2 lines with QC documentation and technical support. Fzd2 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 2 Fzd2 models available — including Conditional Knockout, 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 Fzd2 knockout mouse has the Fzd2 gene permanently inactivated, enabling loss of function studies. A Fzd2 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Fzd2, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Fzd2 organized by modification type. Each URL is indexable and matches common search patterns.