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The aim is to facilitate access for the French research community to the services from the unique national infrastructure and scientific expertise of the PHENOMIN’s partners, and to deliver novel mouse lines that providing important opportunities to advance knowledge gene function in relation to human development and disease. The calls are opened to French research applicants. The project will be submitted to a double-bind review process by an external scientific committee based on the scientific evaluation of the proposal according to the following criteria:

  • The scientific pertinence of the project,
  • The potential to distribute the model under consideration,
  • The innovative nature of the project,
  • The PHENOMIN resources mobilized by the project,
  • The potential publicly availability of the data results.

Request services are done online through our PHENOMIN website. Each applicant will be informed of the outcome of the evaluation within the timing that has been defined for each call. For the calls that are non-free of charge, the cost of the project will be given to the selected applicant for placing an official order.

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Appel à projets INSB | Accès aux Infrastructures Nationales de recherche

Access to Research Infrastructure for state-of-the-art technologies, methods and expertise. – February 2023

We are glad to announce the launch of a new call for proposal INSB CNRS National Infrastructure Access

PHENOMIN - CELPHEDIA is one of the National Infrastructures eligible to this call for proposals offering state-of-the-art technologies, methods and expertise

Program Description:

Click here to view the call on INSB Website


Application Deadline February 28th 2023

Project eligibility and selection criteria:

Click here for the detailed Call

 Results for previous calls

Generation and Characterization of CreERT2 cell specific promoter driven deleter mouse lines.

9 new additional CreERT2 mouse lines are generating by PHENOMIN team and will be made available as soon as possible for the scientific community and 4 CreERT2 mouse models have been already generated by the European EUCOMMTOOLS consortium and and will be further characterized.

More information about this call

Find your model on our MouseCre and CreERT2 Zoo !


Creation and exploration of mouse models for rare diseases.

The French Foundation for rare diseases "Fondation maladies rares" and the French National Infrastructures PHENOMIN and CELPHEDIA launched 1 join call "new experimental animal models of rare diseases" (2019), and 3 successive joint calls "Mouse models and rare diseases" (in 2017, 2015 and 2013, respectively) to give a significant boost to the development of mouse models, in order to i) gain a better understanding of the pathophysiological mechanisms involved in rare diseases whose defective genes have been identified, ii) Test and validate therapeutic proofs of concept, at the pre-clinical in vivo level. 50 projects for new mouse models and 3 projects for new rat models have been or are being realized from 145 submissions.

More information about theses calls


Find you mouse model for rare disease among our available models !



Conditional or constitutive knock-out mouse generation and standard phenotyping.


       More information about this call

More information about this call

More information about this call

More information about this call


New mouse models are available and/or in the process of being generated !