MitoMatcher – Summary Dashboard

MitoMatcher is a database dedicated to the description and analysis of mitochondrial genome variations observed in various clinical and biological contexts. The data presented on this page originate from the Mitomatcher database and are strictly aggregated and non-identifiable. No information allowing direct or indirect identification of individuals is displayed. The aim is to provide a clear and educational overview of the database content, accessible to clinicians, researchers, and anyone interested in mitochondrial data.

MitoMatcher Summary Dashboard offers a global view of the data currently available, including variant types, sample distributions, general clinical characteristics, and associated metadata. This page is not intended as a diagnostic tool, but rather as an exploratory and informative interface to better understand the Mitomatcher database.

Café Variome - MitoMatcher is a discovery module web-based component designed to enable secure discovery and sharing of genomic variant data across institutions. It allows authorized users to query MitoMatcher data, identify matching variants or phenotypes, and facilitate collaboration between clinical and research centers while preserving patient privacy through controlled access and authentication mechanisms.

Key figures

Last update 28/05/2026
Patients 8752
Patients with clinical data 2103
Samples 10669
Mutations 5893
Affected genes 37
Haplogroups 21

Summary Dashboard

Gender distribution

Age of onset

Clinical manifestations

Samples

Haplogroups

Pathogenic variants

People behind MitoMatcher database

Contacts

For scientific questions related to the Mitomatcher database:

This page does not provide medical advice and must not be used for diagnosis.