MT-ND6 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	MT-ND6
Gene name	mitochondrially encoded NADH dehydrogenase 6
Chromosome	M
Chromosomal band	M
Imprinted
Genomic reference	NC_012920.1
Transcript reference	MT-ND6-201
Associated with diseases	553000, LDYT, , , LHON, MELAS SYNDROME
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	43
Unique public DNA variants reported	43
Individuals with public variants	0
Hidden variants	0
Download all this gene's data	Download all data
Notes	MSeqDR-LSDB
Date created	November 12, 2013
Date last updated	November 30, -0001
Version	MT-ND6:-11130

Graphical displays and utilities
Graphs	Graphs displaying summary information of all variants in the database »
UCSC Genome Browser	Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser	Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer	Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC	7462
Entrez Gene	4541
PubMed articles	MT-ND6
OMIM - Gene	516006
OMIM - Diseases	553000 (ONCOCYTOMA ) LDYT (LEBER OPTIC ATROPHY AND DYSTONIA, alt: LEBER HEREDITARY OPTIC NEUROPATHY WITH DYSTONIA) LHON (LEBER OPTIC ATROPHY, LEBER HEREDITARY OPTIC NEUROPATHY) MELAS SYNDROME (MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES)
HGMD	MT-ND6
GeneCards	MT-ND6
GeneTests	MT-ND6

Active transcripts

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00001348	M	MT-ND6-201	MT-ND6-201	-	43

Copyright & disclaimer
Mitochondria chromosome located genes from HGNC

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium