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Early-onset Parkinson disease

Gene: MT-ND6

No list
MT-ND6 (mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6)
EnsemblGeneIds (GRCh38): ENSG00000198695
EnsemblGeneIds (GRCh37): ENSG00000198695
OMIM: 516006, Gene2Phenotype
MT-ND6 is in 4 panels

1 review

SHEKEEB MOHAMMAD (Children's Hospital at Westmead)

Green List (high evidence)

Sources: Literature
Created: 22 Jul 2022, 6:53 a.m.

Mode of inheritance
MITOCHONDRIAL

Phenotypes
Leber Optic Atrophy; Parkinsonism; OMIM 516006

Publications

Created: 22 Jul 2022, 6:53 a.m.

Panel version: 0.215

Details

Mode of Inheritance
MITOCHONDRIAL
Sources
Phenotypes
  • Leber Optic Atrophy
  • Parkinsonism
  • OMIM 516006
Tags
mtDNA
OMIM
516006
Clinvar variants
Variants in MT-ND6
Penetrance
None
Publications
Panels with this gene

History Filter Activity

26 Jul 2022, Gel status: 0

Added Tag

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Tag mtDNA tag was added to gene: MT-ND6.

22 Jul 2022, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

SHEKEEB MOHAMMAD (Children's Hospital at Westmead)

gene: MT-ND6 was added gene: MT-ND6 was added to Early-onset Parkinson disease. Sources: Literature Mode of inheritance for gene gene: MT-ND6 was set to MITOCHONDRIAL Publications for gene: MT-ND6 were set to PMID: 33109474 Phenotypes for gene: MT-ND6 were set to Leber Optic Atrophy; Parkinsonism; OMIM 516006 Review for gene: MT-ND6 was set to GREEN