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
Database search
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.