COL17A1

collagen type XVII alpha 1 chain
OMIM: 113811, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green COL17A1 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.10

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epithelial recurrent erosion dystrophy, MIM# 122400

Green COL17A1 in Epidermolysis bullosa


Level 2: Dermatological disorders
Version 1.15

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epidermolysis bullosa, junctional, localisata variant, MIM# 226650
  • Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650
  • Epithelial recurrent erosion dystrophy, MIM# 122400

Green COL17A1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Epidermolysis bullosa, junctional 4, intermediate MIM#619787
  • Epithelial recurrent erosion dystrophy MIM#122400
  • Amelogenesis imperfecta MONDO:0019507, COL17A1-related

Green COL17A1 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)

Green COL17A1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Epidermolysis bullosa, junctional, non-Herlitz type

Green COL17A1 in Amelogenesis imperfecta


Level 2: Skeletal disorders
Version 1.10

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Epidermolysis bullosa, junctional, non-Herlitz type, MIM#226650 (includes enamel pitting)
  • Amelogenesis imperfecta MONDO:0019507, COL17A1-related

Green COL17A1 in Prepair 1000+


Level 2: Screening
Version 1.9

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)

Red COL17A1 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category A gene
Phenotypes
  • Epidermolysis bullosa, junctional 4, intermediate MIM#619787

Green COL17A1 in Prepair 500+


Level 2: Screening
Version 1.1

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)