Corneal dystrophies

Gene: DCN

Green List (high evidence)

DCN (decorin)
EnsemblGeneIds (GRCh38): ENSG00000011465
EnsemblGeneIds (GRCh37): ENSG00000011465
OMIM: 125255, Gene2Phenotype
DCN is in 3 panels

1 review

Morag Shanks (Oxford Medical Genetics laboratory)

Green List (high evidence)

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • Corneal dystrophy, congenital stromal 610048
OMIM
125255
Clinvar variants
Variants in DCN
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Apr 2019, Gel status: 4

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

Ivone Leong (Genomics England Curator)

gene: DCN was added gene: DCN was added to Corneal dystrophies. Sources: Wessex and West Midlands GLH,Expert Review Green Mode of inheritance for gene: DCN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: DCN were set to 24413633; 15671264; 16935612 Phenotypes for gene: DCN were set to Corneal dystrophy, congenital stromal 610048