Incidentalome_PREGEN_DRAFT

Gene: DSC2

Green List (high evidence)

DSC2 (desmocollin 2)
EnsemblGeneIds (GRCh38): ENSG00000134755
EnsemblGeneIds (GRCh37): ENSG00000134755
OMIM: 125645, Gene2Phenotype
DSC2 is in 11 panels

1 review

Tony Roscioli (New South Wales Health Pathology)

Red List (low evidence)

A cause of a Mendelian disorder that could present in fetal life or childhood
Created: 4 Dec 2020, 4:30 a.m. | Last Modified: 4 Dec 2020, 4:30 a.m.
Panel Version: 0.3

History Filter Activity

9 Nov 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: DSC2 was added gene: DSC2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: DSC2 was set to Unknown