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  2. Gastrointestinal epithelial barrier disorders
  3. MAGI2
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Gastrointestinal epithelial barrier disorders

Gene: MAGI2

Red List (low evidence)
MAGI2 (membrane associated guanylate kinase, WW and PDZ domain containing 2)
EnsemblGeneIds (GRCh38): ENSG00000187391
EnsemblGeneIds (GRCh37): ENSG00000187391
OMIM: 606382, Gene2Phenotype
MAGI2 is in 5 panels

1 review

Olivia Niblock (Genomics England Curator)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
Celiac Disease; IBD

Publications

Created: 21 Jul 2017, 1:55 p.m.

Panel version: 0.8

Details

Mode of Inheritance
Unknown
Sources
  • Literature
Phenotypes
  • Celiac Disease
  • IBD
  • IBD
OMIM
606382
Clinvar variants
Variants in MAGI2
Penetrance
Complete
Publications
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 MAGI2 were set to Celiac Disease, IBD, IBD

21 Jul 2017, Gel status: 0

Created

Olivia Niblock (Genomics England Curator)

MAGI2 was created by oniblock

21 Jul 2017, Gel status: 0

Added New Source

Olivia Niblock (Genomics England Curator)

MAGI2 was added to Gastrointestinal epithelial barrier disorderspanel. Sources: Literature