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  2. Gastrointestinal epithelial barrier disorders
  3. IRGM
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Gastrointestinal epithelial barrier disorders

Gene: IRGM

Red List (low evidence)
IRGM (immunity related GTPase M)
EnsemblGeneIds (GRCh38): ENSG00000237693
EnsemblGeneIds (GRCh37): ENSG00000237693
OMIM: 608212, Gene2Phenotype
IRGM is in 2 panels

0 reviews

Details

Sources
  • Other
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Inflammatory bowel disease 19, 612278
  • Crohn disease
  • {Inflammatory bowel disease (Crohn disease) 19}
OMIM
608212
Clinvar variants
Variants in IRGM
Penetrance
None
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

Added New Source, Set penetrance

Olivia Niblock (Genomics England Curator)

Other was added to IRGM. Panel: Gastrointestinal epithelial barrier disorders Phenotypes for gene IRGM were set to Inflammatory bowel disease 19, 612278, Crohn disease, {Inflammatory bowel disease (Crohn disease) 19}

17 Apr 2018, Gel status: 1

Added New Source

Olivia Niblock (Genomics England Curator)

IRGM was added to Gastrointestinal epithelial barrier disorders panel. Sources: Radboud University Medical Center, Nijmegen

17 Apr 2018, Gel status: 1

Created

Olivia Niblock (Genomics England Curator)

IRGM was created by Olivia Niblock