Gastrointestinal epithelial barrier disorders
Gene: MYO9B
MYO9B (myosin IXB)
EnsemblGeneIds (GRCh38): ENSG00000099331
EnsemblGeneIds (GRCh37): ENSG00000099331
OMIM: 602129, Gene2Phenotype
MYO9B is in 3 panels
EnsemblGeneIds (GRCh38): ENSG00000099331
EnsemblGeneIds (GRCh37): ENSG00000099331
OMIM: 602129, Gene2Phenotype
MYO9B is in 3 panels
1 review
Olivia Niblock (Genomics England Curator)
Comment on list classification: From internal clinical team review: this appears to be a risk allele for coeliac disease and is unlikely to be useful for patients recruited under this category. Therefore, gene remains as low evidence.Created: 25 Jul 2018, 3:08 p.m.
Mode of inheritance
Unknown
Phenotypes
Celiac Disease
Publications
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Literature
- Phenotypes
-
- Celiac Disease
- OMIM
- 602129
- Clinvar variants
- Variants in MYO9B
- 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
25 Jul 2018, Gel status: 1
Entity classified by Genomics England curator
Olivia Niblock (Genomics England Curator)Gene: myo9b has been classified as Red List (Low Evidence).
17 Apr 2018, Gel status: 1
Set penetrance
Olivia Niblock (Genomics England Curator)Phenotypes for gene MYO9B were set to Celiac Disease
21 Jul 2017, Gel status: 0
Created
Olivia Niblock (Genomics England Curator)MYO9B was created by oniblock
21 Jul 2017, Gel status: 0
Added New Source
Olivia Niblock (Genomics England Curator)MYO9B was added to Gastrointestinal epithelial barrier disorderspanel. Sources: Literature