Structural basal ganglia disorders
Gene: MT-ND1EnsemblGeneIds (GRCh38): ENSG00000198888
EnsemblGeneIds (GRCh37): ENSG00000198888
OMIM: 516000, Gene2Phenotype
MT-ND1 is in 11 panels
5 reviews
Carl Fratter (Oxford University Hospitals NHS Trust)
Mode of inheritance
MITOCHONDRIAL
Variants in this GENE are reported as part of current diagnostic practice
Sarah Leigh (Genomics England Curator)
Comment on list classification: Green on Version 1 Mitochondrial disorders panelCreated: 2 Mar 2017, 1:48 p.m.
Manju Kurian (UCL-Institute of Child Health)
Mode of inheritance
MITOCHONDRIAL
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Both reviewers agree this gene should be promoted from red to green.
Created: 10 Feb 2016, 12:52 p.m.
Shamima Rahman (UCL Institute of Child Health)
Details
- Mode of Inheritance
- MITOCHONDRIAL
- Sources
-
- Expert Review Green
- Tags
- OMIM
- 516000
- Clinvar variants
- Variants in MT-ND1
- Penetrance
- Complete
- Panels with this gene
-
- Sudden death in young people
- Structural basal ganglia disorders
- Undiagnosed metabolic disorders
- Mitochondrial disorders
- Adult onset dystonia, chorea or related movement disorder
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Optic neuropathy
- Likely inborn error of metabolism
- Retinal disorders
- Leber hereditary optic neuropathy
History Filter Activity
Removed Tag
Achchuthan Shanmugasundram (Genomics England Curator)Tag limit of detection for heteroplasmic variants is not validated for WGS testing was removed from gene: MT-ND1.
Added Tag
Achchuthan Shanmugasundram (Genomics England Curator)Tag limit of detection for heteroplasmic variants is not validated for WGS testing tag was added to gene: MT-ND1.
Added Tag
Eleanor Williams (Genomics England Curator)Tag gene-checked tag was added to gene: MT-ND1.
panel promoted to version 1
Sarah Leigh (Genomics England Curator)promoted 16/03/2017
Gene classified by Genomics England curator
Sarah Leigh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Manju Kurian (UCL-Institute of Child Health)MT-ND1 was added to Structural basal ganglia disorderspanel. Sources: Literature
Created
Manju Kurian (UCL-Institute of Child Health)MT-ND1 was created by Manju