AlphaFold predicted structure
MT-ND6 · P03923

Mean pLDDT
84.8/ 100
Confident
174 residues
Confidence breakdown
- Very high(≥ 90)52%
- Confident(70–90)36%
- Low(50–70)5%
- Very low(< 50)7%
AlphaFold (Jumper et al., 2021) · CC BY 4.0
mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6
Annotations refreshed 1 month ago.
Diagnostic Grade (Green)
Likely inborn error of metabolism
MITOCHONDRIALMitochondrial disorders
MITOCHONDRIALOptic neuropathy
MITOCHONDRIALStructural basal ganglia disorders
MITOCHONDRIALUndiagnosed metabolic disorders
MITOCHONDRIALAdult onset dystonia, chorea or related movement disorder
MITOCHONDRIALAdult onset neurodegenerative disorder
MITOCHONDRIALAlbinism or congenital nystagmus
MITOCHONDRIAL+6 more panels — install the extension to see the full list inline on any page.
Leber hereditary optic neuropathy
Leigh syndrome
MELAS syndrome
mitochondrial disease
MELAS
type 2 diabetes mellitus
diabetes mellitus
Leber plus disease
mitochondrial myopathy with reversible cytochrome C oxidase deficiency
polycystic ovary syndrome
Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.
NADH-ubiquinone oxidoreductase chain 6
Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor (PubMed:14595656, PubMed:8644732). Essential for the catalytic activity and assembly of complex I (PubMed:14595656, PubMed:8644732)
Curated MONDO disease pages that list MT-ND6 among their top associated genes.
MT-ND6 · P03923

Mean pLDDT
84.8/ 100
Confident
174 residues
Confidence breakdown
AlphaFold (Jumper et al., 2021) · CC BY 4.0