Selected-GenAtlas references SOURCE GeneCards NCBI Gene Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol MT-ND6 contributors: shn - updated : 13-11-2012
HGNC name mitochondrially encoded NADH dehydrogenase 6
HGNC id 7462
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
HOMOLOGY
interspecies ortholog to ND6, Pan troglodytes
ortholog to Nd6, Mus musculus
ortholog to Nd6, rattus norvegicus
Homologene
FAMILY complex I subunit 6 family
CATEGORY enzyme
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,organelle,mitochondria,inner
intracellular,cytoplasm,organelle,membrane
text mitochondrial inner membrane
CELLULAR PROCESS
PHYSIOLOGICAL PROCESS respiration
text mitochondrial respiratory chain enzyme
PATHWAY
metabolism
signaling
a component
INTERACTION
DNA
RNA
small molecule
protein
cell & other
REGULATION
ASSOCIATED DISORDERS
corresponding disease(s) LHON , MTENC2
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional somatic mutation      
Leber's hereditary optic neuropathy (LHON) is associated with the mitochondrial ND6 T14484C mutation in three Chinese families
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
Mice with mtDNA ND6 P25L mutation display reduction in retinal function by elecroretinogram, age-related decline in central smaller caliber optic nerve fibers with sparing of larger peripheral fibers, neuronal accumulation of abnormal mitochondria, axonal swelling, and demyelination mostly due to oxidative stress