- About
- MSeqDR-LSDB
- Tools
- mtDNA Tool:
- mvTool
- Phy-Mer
- MToolBox
- mvTool for Haplogroup
- mvTool with HmtDB
- MitoMaster
- MitoTIP tRNA Scoring
- MSeq-OpenCGA
- Variant Tool:
- VariantOneStop
- Quick-Mitome
- Quick-Mitome-Report
- HBCR Exome (Retired)
- POLG Patho. Server
- Data - Awsomics GeEx
- Expert Panel
- Panel Tool:
- Gene Panel Examiner
- Transgenomic_NuclearMitome
- Pedigree Maker
- json2table
-
Phenome
- Disease Portal
- HPO Ontology Browser
- Core Symptoms (draft)
- NAMDC-HPO Mapping (retired)
- Expert Panel
- Clinical
- Overview
- Leigh Syndrome Resource
- Collaboration
- Submission
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Examples Gene: MT-ND1, POLG,
Region: M:1-1000
Variant: m.8993T>G, 1:g.10042757T>C
rs3888511 MSCV_0000006,
ClinVar: RCV000000015,
Disease: Leigh syndrome,
Phenotype: Retinopathy
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