Dystonia - childhood onset

Gene: DRD2

Red List (low evidence)

DRD2 (dopamine receptor D2)
EnsemblGeneIds (GRCh38): ENSG00000149295
EnsemblGeneIds (GRCh37): ENSG00000149295
OMIM: 126450, Gene2Phenotype
DRD2 is in 7 panels

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Details

History Filter Activity

9 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Louise Daugherty (Genomics England Curator)

Eleanor Williams: Updated to green when making t

19 Dec 2018, Gel status: 1

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

Eleanor Williams (Genomics England Curator)

gene: DRD2 was added gene: DRD2 was added to Dystonia - childhood onset. Sources: Expert Review Red Mode of inheritance for gene: DRD2 was set to Unknown Publications for gene: DRD2 were set to 20301587 Phenotypes for gene: DRD2 were set to Dystonia, myoclonic, 159900