• Cite IMPC
  • Help
  • IMPC Cloud
  • Contact us
  • About the IMPC
  • Data
  • Human Diseases
  • Publications
  • News
  • Blog
Genes Phenotypes Everything Else

About the IMPC

Consortium Members

Collaborations

Funding

Animal Welfare

About KOMP

Data

COVID-19 Resources

Getting Started with IMPC Data

IMPC Data Generation

How to Use Gene Pages

Citing IMPC Data

Allele design

IMPC Data Collections

Late Adult Data

Histopathology

Essential genes

Embryo Development

Cardiovascular

Accessing the Data

Latest Data Release

Access via API

Access via FTP

Batch query

Advanced Tools

PhenoDCC Tools

GenTaR

OpenStats

IMPReSS

Embryo Viewer

Human Diseases

Publications

Latest IMPC Papers

Data Supporting IMPC Papers

Pain Sensitivity Associated Genes

Essential Genes - Linking to Disease

Essential Genes - Translating to Other Species

Sexual Dimorphism

Genes Critical for Hearing Identified

Genetic Basis for Metabolic Diseases

Papers Using IMPC Resources

News

Blog

Help

IMPC Cloud

Contact us

About the IMPC Consortium Members Collaborations Funding Animal Welfare About KOMP
COVID-19 Resources
Getting Started with IMPC Data

IMPC Data Generation

How to Use Gene Pages

Citing IMPC Data

Allele design

IMPC Data Collections

Late Adult Data

Histopathology

Essential genes

Embryo Development

Cardiovascular

Accessing the Data

Latest Data Release

Access via API

Access via FTP

Batch query

Advanced Tools

PhenoDCC Tools

GenTaR

OpenStats

IMPReSS

Embryo Viewer

Latest IMPC Papers
Data Supporting IMPC Papers

Pain Sensitivity Associated Genes

Essential Genes - Linking to Disease

Essential Genes - Translating to Other Species

Sexual Dimorphism

Genes Critical for Hearing Identified

Genetic Basis for Metabolic Diseases

Papers Using IMPC Resources

Dev data warning:

You are currently visiting the dev server for the IMPC. This site is unstable and is displaying test data. To access the live data from the IMPC please visit https://www.mousephenotype.org

Genes Phenotypes Help, News, Blog
Home Blog External Paper
Blog Posts
Researchers Investigate The Cause Of Fam151b-Related Retinal Degeneration

Researchers Investigate the Cause of Fam151b-related Retinal Degeneration

Researchers at the MRC Human Genetics Unit (Institute for Genetics and Molecular Medicine, University of Edinburgh) collaborated with the Mary…

Published: 12 Oct 2020

Steroid Biosynthesis Pathway Could Be Targeted To Reactivate Anti-Tumour Immunity

Steroid Biosynthesis Pathway Could Be Targeted to Reactivate Anti-tumour Immunity

Guest blog post by Bidesh Mahata. Bidesh Mahata is a newly recruited group leader in the Division of Immunology, Department…

Published: 17 Jul 2020

Gene Found for BCAA Clearance in Brown Fat Protects Against Obesity & Diabetes

Branched-chain amino acids (BCAAs) are amino acids that have a central carbon atom with a branch of three or more…

Published: 25 Jun 2020

Researchers Study Biomarker Patterns to Define the Start of Ageing

Scientists worldwide are still attempting to define ageing and mortality through research. Debate on ageing continues to vary widely and…

Published: 19 May 2020

Arf1-KO Induces Anti-Tumour Response with Protective Vaccination

A study investigating the role of Arf1 shows promising results for new therapeutic strategies involving DAMP-mediated anti-tumour immunity to target…

Published: 27 Apr 2020

Brain (correct size)

Study Uncovers 198 Genes Associated With Brain Morphogenesis in Mice

With a contribution from the IMPC, recent research, published in Nature Communications, has identified 198 genes associated with brain morphogenesis…

Published: 4 Oct 2019

Knockout Mouse Model Reveals Insight into Traits Associated With PCD

Members of the IMPC Consortium at CNR-Monterotondo (Italy) have used embryonic stem (ES) cells produced as part of the IMPC…

Published: 16 Aug 2019

PIK3CA inhibition with BYL719 – a novel treatment for CLOVES syndrome

CLOVES syndrome is a rare condition that is characterised by tissue overgrowth and vascular abnormalities, caused by mosaic gain-of-function mutations…

Published: 3 Jul 2019

SETD3 – An Actin Methyltransferase That Prevents Primary Dystocia

Research published in Nature identifies SET domain protein 3 (SETD3) as a physiological actin methyltransferase, and uncovers SETD3’s crucial role…

Published: 20 May 2019

Research Reveals Novel Genetic Influences On Osteoporosis

Recent research, published in nature genetics, identifies novel genetic influences on osteoporosis, with the potential to empower future research on…

Published: 19 Mar 2019

Popular on IMPC

Search our portal for mouse resources of lasting biological value

Genes Phenotypes

Twitter

Tweets by impc

Content on this site is licensed under a Creative Commons Attribution 4.0 International license

Privacy & CookiesTerms of use

  • About the IMPC
  • Data
  • Human Diseases
  • Publications
  • News
  • Blog
  • Cite IMPC
  • Help
  • IMPC Cloud
  • Contact us
  • IMPC Twitter
  • IMPC YouTube
  • IMPC Facebook
  • IMPC Reddit
Access Latest Data Release Data
  • Batch query
  • Access via API
  • Access via FTP