Gastrointestinal epithelial barrier disorders

Gene: ATG16L1

Red List (low evidence)

ATG16L1 (autophagy related 16 like 1)
EnsemblGeneIds (GRCh38): ENSG00000085978
EnsemblGeneIds (GRCh37): ENSG00000085978
OMIM: 610767, Gene2Phenotype
ATG16L1 is in 3 panels

0 reviews


  • Other
  • {Inflammatory bowel disease (Crohn disease) 10}
  • Crohn disease
Clinvar variants
Variants in ATG16L1
Panels with this gene

History Filter Activity

25 Jul 2018, Gel status: 1

Panel promoted to version 1.0

Olivia Niblock (Genomics England Curator)

Panel reviews have been assessed and internal clinical team opinion has been sought on this panel, particularly to rule out incidental findings. Panel has been revised through expert review, internal review and literature research. 25/07/2018

17 Apr 2018, Gel status: 1

Set penetrance

Olivia Niblock (Genomics England Curator)

Phenotypes for gene ATG16L1 were set to {Inflammatory bowel disease (Crohn disease) 10}, Crohn disease

17 Apr 2018, Gel status: 1

Added New Source

Olivia Niblock (Genomics England Curator)

ATG16L1 was added to Gastrointestinal epithelial barrier disorders panel. Sources: Other

17 Apr 2018, Gel status: 1


Olivia Niblock (Genomics England Curator)

ATG16L1 was created by Olivia Niblock