Early onset dystonia
Gene: PARK7Comment on list classification: Discussed internally, and the decision was made to not include this on the dystonia panel.Created: 2 Sep 2016, 11:40 a.m.
Comment on list classification: Multiple cases with Parkinson disease 7, autosomal recessive early-onset reported on OMIM for multiple different variants in this gene.Created: 23 Aug 2016, 2:23 p.m.
Comment on list classification: Promoted from red to green due to feedback from Huw Morris (UCL).Created: 19 Aug 2016, 9:26 a.m.
Comment on list classification: Is on the Parkinson's Disease NGS Panel in the UCLH National Hospital for Neurology and Neurosurgery & Institute of Neurology (NHNN) Neurogenetics genetic testing manual.Created: 10 Jun 2016, 8:19 a.m.
17th Oct 2016: Promoted to version 1. The panel was revised after expert input and internal discussion with the clinical team. Other panels such as hereditary ataxia or dementia may be applied in conjunction with this panel where appropriate for genome analysis.
This gene has been classified as Red List (Low Evidence).
This gene has been classified as Red List (Low Evidence).
This gene has been classified as Green List (High Evidence).
This gene has been classified as Green List (High Evidence).
This gene has been classified as Green List (High Evidence).
PARK7 was created by ellenmcdonagh
PARK7 was added to Early onset dystoniapanel. Sources: Expert Review