Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The knockout mouse project.

Christopher P Austin1, James F Battey, Allan Bradley

  • 1National Human Genome Research Institute, National Institutes of Health, Building 31, Room 4B09, 31 Center Drive, Bethesda, Maryland 20892, USA. austinc@mail.nih.gov

Nature Genetics
|September 2, 2004
PubMed
Summary

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A disease model resource reveals core principles of tissue-specific cancer evolution.

Nature·2026
Same author

A forward genetic screen identifies potassium channel essentiality in SHH medulloblastoma maintenance.

Developmental cell·2025
Same author

Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines.

Scientific reports·2024
Same author

<i>In vivo</i> interrogation of regulatory genomes reveals extensive quasi-insufficiency in cancer evolution.

Cell genomics·2023
Same author

Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoire.

PloS one·2022
Same author

Cas9-induced large deletions and small indels are controlled in a convergent fashion.

Nature communications·2022
Same journal

Mutational scanning reveals substrate-assisted autoregulation of the WNT destruction complex.

Nature genetics·2026
Same journal

Spatial transcriptomic analyses highlight distinct erythroid niches in mice and humans.

Nature genetics·2026
Same journal

Building up pangenome analysis block by block.

Nature genetics·2026
Same journal

Mutations in splicing factor gene U2AF1 rescue defective oncogene splicing in KRAS-mutant cancers.

Nature genetics·2026
Same journal

Assessing the effect of immune surveillance on clonal expansions in the blood.

Nature genetics·2026
Same journal

Improved heritability partitioning and enrichment analyses using summary statistics with graphREML.

Nature genetics·2026
See all related articles
This summary is machine-generated.

Creating a comprehensive, publicly available collection of mouse knockouts is crucial for advancing biomedical research. This high-throughput effort will standardize gene function studies and accelerate biological discovery.

Area of Science:

  • Genetics and Genomics
  • Molecular Biology
  • Biomedical Research

Background:

  • Mouse knockout technology is essential for understanding gene function in vivo.
  • Currently, only about 10% of mouse genes have published knockouts.
  • Existing knockouts often lack standardization in creation and phenotyping, limiting their utility and availability.

Purpose of the Study:

  • To advocate for a global, high-throughput initiative to generate knockouts for all mouse genes.
  • To emphasize the need for standardized phenotyping and public accessibility of these genetic resources.
  • To accelerate biomedical discovery through comprehensive and accessible mouse knockout models.

Main Methods:

  • Leveraging new technologies and production efficiencies for high-throughput knockout generation.

Related Experiment Videos

  • Implementing standardized phenotyping protocols across all generated knockouts.
  • Establishing a public domain repository for all mouse knockout resources.
  • Main Results:

    • A significant gap exists in the availability of characterized mouse knockouts for most genes.
    • Current resources are often not standardized or publicly accessible, hindering research.
    • A coordinated international effort is proposed to overcome these limitations.

    Conclusions:

    • A genome-wide collection of standardized, publicly available mouse knockouts is needed.
    • This resource will significantly enable and accelerate biomedical discovery.
    • Harnessing new technologies is key to achieving this goal efficiently.