About
News
Team
U24 Grant
Documentation
Tutorial
UMDF'17 Workshop
UMDF'17 Regional Symposia St Louis
UMDF'16 Workshop
UMDF'15 Workshop
SIMD'15 Workshop
Collaboration Zone
Book: Mitochondrial Disease Genes Compendium
Contact & Feedback
MSeqDR-LSDB
Genes View
Transcripts
Mitochondrial Disease
Genomic Variants
Add
Transcript Variants
LSDB Status
Advanced Users
Tools
Quick-Mitome for WES
Quick-Mitome
Quick-Mitome Report
mtDNA Tool:
mvTool
Phy-Mer
MToolBox
mvTool for Haplogroup
mvTool with HmtDB
MitoMaster
MitoTIP tRNA Scoring
MSeq-OpenCGA
Variant Tool:
VariantOneStop
HBCR Exome (Retired)
POLG Patho. Server
Data - Awsomics GeEx
Expert Panel
Panel Tool:
Gene Panel Examiner
Transgenomic_NuclearMitome
Pedigree Maker
json2table
Phenome-Disease
Disease Portal
Disease Portal in Mondo
HPO Ontology Browser
Leigh Syndrome Resource
Clinical_Portal
PMD Virtual Registry
Collaboration
Genesis (GEM.App)
LeighMap
Expert Panel
Collaboration Zone
--
Overview
--
Login
--
Register
--
MSeqDR_General
Submission
Submit_Interpret_Variant
Instructions
Hello! Guest! Please
Login
or
Register
!
Clinician Mode
Genomic Search
Disease: OMIM
Disease: HPO
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
Log in needed to continue...
The page you attempted to access is only available to registered users. Please log in or
register
to enjoy your own MSeqDR.
Benefits of Registration:
Submit data through Submission Tool
View your private data and group protected data
Create and modify groups and data acess
Update your personal information
Account:
MSeqDR
Login ID:
Password:
Create MSeqDR account with LinkedIn profile
New User Register
Forget your password?