Genes in panel

Ataxia and cerebellar anomalies - narrow panel

Gene: PDYN

Green List (high evidence)

PDYN (prodynorphin)
EnsemblGeneIds (GRCh38): ENSG00000101327
EnsemblGeneIds (GRCh37): ENSG00000101327
OMIM: 131340, Gene2Phenotype
PDYN is in 9 panels

0 reviews

History Filter Activity

9 Jan 2019, Gel status: 4

Panel promoted to version 1.0

Louise Daugherty (Genomics England Curator)

Checked against super panel made up of the panel constituents. Ready to promote to version 1.

19 Dec 2018, Gel status: 4

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

Ellen McDonagh (Genomics England Curator)

gene: PDYN was added gene: PDYN was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: PDYN was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: PDYN were set to Spinocerebellar ataxia 23