VCAN:Ensemblv115

versican
OMIM: 118661, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green VCAN in Syndromic Retinopathy


Level 2: Ophthalmological disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • RetNet
  • Expert Review Green
Phenotypes
  • Wagner Syndrome

Green VCAN in Vitreoretinopathy


Level 2: Ophthalmological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
Phenotypes
  • Wagner syndrome 1, MIM# 143200
Tags
  • SV/CNV