ATG16L1

autophagy related 16 like 1
OMIM: 610767, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red ATG16L1 in Gastrointestinal epithelial barrier disorders

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.75

review Not set
Sources
  • Other
Phenotypes
  • {Inflammatory bowel disease (Crohn disease) 10}
  • Crohn disease
Amber ATG16L1 in COVID-19 research


Level 2: Viral research
Version 1.142

review Unknown
Sources
  • Expert Review Amber
  • Expert list
  • OMIM
Red ATG16L1 in Severe Paediatric Disorders


Version 1.184

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Next Generation Children Project
  • Expert Review Red
  • Expert list