Over the last decade, new sequencing technologies have enabled the discovery of numerous new disease-associated genes. However, for many genes we still know very little about their function and potential role in disease and many patients remain undiagnosed. Model organisms facilitate the exploration of genotype to phenotype associations and public databases of this knowledge allow us to assess genes with no previous involvement in human disease. Towards this goal, the International Mouse Phenotyping Consortium (IMPC) is building the first complete functional catalogue of the mammalian genome by producing and phenotyping a knockout mouse strain for every protein coding gene.

Analysis of mammalian gene function through mouse phenotyping

2019

Abstract

Over the last decade, new sequencing technologies have enabled the discovery of numerous new disease-associated genes. However, for many genes we still know very little about their function and potential role in disease and many patients remain undiagnosed. Model organisms facilitate the exploration of genotype to phenotype associations and public databases of this knowledge allow us to assess genes with no previous involvement in human disease. Towards this goal, the International Mouse Phenotyping Consortium (IMPC) is building the first complete functional catalogue of the mammalian genome by producing and phenotyping a knockout mouse strain for every protein coding gene.
2019
Istituto di Biochimica e Biologia Cellulare - IBBC
Inglese
51st European Society of Human Genetics Conference: Oral Presentations
51st European Society of Human Genetics Conference
27
770
770
https://doi.org/10.1038/s41431-019-0407-4
Sì, ma tipo non specificato
June 16-19, 2018
Milano
mouse mutant
disease model
2
none
Smedley, D; IMPC KOMPIPADMD Data WGroup,
273
info:eu-repo/semantics/conferenceObject
04 Contributo in convegno::04.01 Contributo in Atti di convegno
   Research Infrastructures for Phenotyping, Archiving and Distribution of Mouse Disease Models - Promoting International Cooperation and User Engagement to Enhance Biomedical Innovation
   IPAD-MD
   H2020
   653961
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/425917
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