This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: MOGS
MOGS (mannosyl-oligosaccharide glucosidase)
EnsemblGeneIds (GRCh38): ENSG00000115275
EnsemblGeneIds (GRCh37): ENSG00000115275
OMIM: 601336, Gene2Phenotype
MOGS is in 10 panels
EnsemblGeneIds (GRCh38): ENSG00000115275
EnsemblGeneIds (GRCh37): ENSG00000115275
OMIM: 601336, Gene2Phenotype
MOGS is in 10 panels
0 reviews
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert list
- Expert Review Green
- Phenotypes
-
- Bacterial and viral infections
- Severe hypogammaglobulinaemia
- Severe neurologic disease
- Congenital disorder of glycosylation, type IIb, MIM#606056
- OMIM
- 601336
- Clinvar variants
- Variants in MOGS
- Penetrance
- None
- Publications
- Panels with this gene
-
- Likely inborn error of metabolism
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Intellectual disability
- Early onset or syndromic epilepsy
- COVID-19 research
- Undiagnosed metabolic disorders
- Fetal anomalies
- DDG2P
- Congenital disorders of glycosylation
- Childhood onset dystonia, chorea or related movement disorder
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: MOGS was added gene: MOGS was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Expert Review Green,Expert list Mode of inheritance for gene: MOGS was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MOGS were set to 24716661; 29235540; 10788335 Phenotypes for gene: MOGS were set to Bacterial and viral infections; Severe hypogammaglobulinaemia; Severe neurologic disease; Congenital disorder of glycosylation, type IIb, MIM#606056