Childhood onset dystonia, chorea or related movement disorder
Gene: PDYN

PDYN (prodynorphin)
EnsemblGeneIds (GRCh38): ENSG00000101327
EnsemblGeneIds (GRCh37): ENSG00000101327
OMIM: 131340, Gene2Phenotype
PDYN is in 8 panels

1 review

James Polke (Neurogenetics Laboratory, Institute of Neurology, London)

I don't know

?include ataxia genes
Created: 9 Jul 2019, 4:24 p.m. | Last Modified: 9 Jul 2019, 4:24 p.m.

Panel Version: 0.9

Created: 9 Jul 2019, 4:24 p.m.
Last Modified: 9 Jul 2019, 4:24 p.m.
Panel version: Imported from GMS Neurology specialist test group-Movement disorders - childhood onset-LNGLH_v2 panel version 0.9

Details

Sources

London North GLH
Expert Review Amber

Phenotypes

Spinocerebellar ataxia 23, 610245

OMIM

131340

Clinvar variants

Variants in PDYN

Penetrance

None

Panels with this gene

History Filter Activity

8 Dec 2019, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for gene: PDYN were changed from to Spinocerebellar ataxia 23, 610245

6 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Ellen McDonagh (Genomics England Curator)

gene: PDYN was added gene: PDYN was added to Childhood onset dystonia or chorea or related movement disorder. Sources: Expert Review Amber,London North GLH Mode of inheritance for gene: PDYN was set to

Childhood onset dystonia, chorea or related movement disorder Gene: PDYN