COL5A1

collagen type V alpha 1 chain
OMIM: 120215, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green COL5A1 in Aortopathy_Connective Tissue Disorders


Level 2: Cardiovascular disorders
Version 1.85

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ehlers-Danlos syndrome, classic type, 1, MIM# 130000
  • Fibromuscular dysplasia, multifocal, MIM# 619329

Amber COL5A1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Ehlers-Danlos syndrome, classic type, MIM# 130000

Green COL5A1 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ehlers-Danlos syndrome, classic type, 1, MIM# 130000
  • Fibromuscular dysplasia, multifocal, MIM# 619329

Red COL5A1 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review Not set
Sources
  • Expert Review Green
  • Expert
  • Victorian Clinical Genetics Services

Green COL5A1 in Ehlers Danlos syndromes


Level 2: Cardiovascular disorders
Version 1.3

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • International EDS Consortium
  • Expert Review Green
Phenotypes
  • Ehlers-Danlos syndrome, classic type, 130000
  • Classical EDS

Green COL5A1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Ehlers-Danlos syndrome, type I

Red COL5A1 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category A gene
Phenotypes
  • Fibromuscular dysplasia, multifocal, MIM# 619329
  • Ehlers-Danlos syndrome, classic type, 1, MIM# 130000