Conventional / global / constitutive KO
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Browse 1 Kctd13 mouse model including knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Kctd13, the mouse ortholog of human KCTD13, encodes a BTB domain protein that functions as a substrate adaptor within Cullin3 RING E3 ubiquitin ligase complexes, with its best-defined substrate being RhoA, whose polyubiquitination and degradation link this locus to actin cytoskeletal dynamics, synapse structure, and neuronal migration. The gene lies within the 16p11.2 interval whose recurrent deletion and duplication cause reciprocal head size and body weight phenotypes together with autism and schizophrenia risk, and KCTD13 has been nominated as a principal dosage-sensitive driver of that interval, although later work argues the phenotype is polygenic within the region. Mouse nulls show reduced synaptic transmission with elevated RhoA and altered spine density, without lethality. The design fork is therefore dosage-focused: conditional nulls test cell-autonomous requirement, while conditional overexpression or duplication alleles model the reciprocal copy number state. Kctd10 and Tnfaip1 share Cullin3 adaptor activity toward RhoA, so quantify RhoA levels rather than assuming complete pathway disinhibition.
ingenious targeting laboratory offers 1 distinct Kctd13 (KCTD13) catalog mouse model, 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 Kctd13 (human KCTD13). Catalog lines ship when inventory exists. Everything else is a generation quote.
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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
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Specify rabbit on quote
Background substrain on quote
Background strain on quote
1 Kctd13 line with QC documentation and technical support.
Kctd13-KO
KnockoutKO/CKO mice
We have 1 Kctd13 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.
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Order catalog modelA Kctd13 knockout mouse has the Kctd13 gene permanently inactivated, enabling loss of function studies.
Jump to catalog backed pages for Kctd13 organized by modification type. Each URL is indexable and matches common search patterns.