MITOBREAK

MITOBREAK catalogs curated mitochondrial DNA (mtDNA) rearrangements across multiple species, reporting breakpoint positions, junction sequences, and associated phenotypic information for circular deletions, circular partially-duplicated duplications, and linear mtDNAs to support research into mtDNA structural alterations and their roles in disease.


Key Features:

  • Comprehensive Database: Contains over 1,400 documented mtDNA rearrangements compiled from nearly 400 publications.
  • Species Coverage: Includes entries from Homo sapiens, Mus musculus, Rattus norvegicus, Macaca mulatta, Drosophila melanogaster, Caenorhabditis elegans, and Podospora anserina.
  • Classes of Rearrangements: Covers three primary classes: circular deletions, circular partially-duplicated duplications, and linear mtDNAs.
  • Phenotypic Information: Annotates each entry with associated phenotypic information.
  • Breakpoint and Junction Details: Documents precise breakpoint positions and junction sequences for reported cases.

Scientific Applications:

  • Mitochondrial Disease Research: Supports investigation of causes and consequences of mitochondrial diseases by providing breakpoint and phenotypic data.
  • Mechanistic Studies of mtDNA Rearrangements: Enables analysis of breakpoints and junction sequences to study mechanisms driving mtDNA structural alterations.
  • Basic and Applied mtDNA Research: Facilitates basic research on mtDNA structure and function and applied investigations toward identifying potential therapeutic targets for mitochondrial disorders.

Methodology:

The source description does not specify computational methods, algorithms, or file formats.

Topics

Details

Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
12/18/2017
Last Updated:
1/15/2019

Operations

Data Inputs & Outputs

Publications

Damas J, Carneiro J, Amorim A, Pereira F. MitoBreak: the mitochondrial DNA breakpoints database. Nucleic Acids Research. 2013;42(D1):D1261-D1268. doi:10.1093/nar/gkt982. PMID:24170808. PMCID:PMC3965124.

Documentation