This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: DOCK8
DOCK8 (dedicator of cytokinesis 8)
EnsemblGeneIds (GRCh38): ENSG00000107099
EnsemblGeneIds (GRCh37): ENSG00000107099
OMIM: 611432, Gene2Phenotype
DOCK8 is in 12 panels
EnsemblGeneIds (GRCh38): ENSG00000107099
EnsemblGeneIds (GRCh37): ENSG00000107099
OMIM: 611432, Gene2Phenotype
DOCK8 is in 12 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Australian Genomics Health Alliance Immunology Flagship
- Victorian Clinical Genetics Services
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- OMIM
- 611432
- Clinvar variants
- Variants in DOCK8
- Penetrance
- None
- Panels with this gene
-
- Familial pulmonary fibrosis
- COVID-19 research
- Fetal anomalies
- DDG2P
- Gastrointestinal epithelial barrier disorders
- Severe multi-system atopic disease with high IgE
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Rare genetic inflammatory skin disorders
- Haematological malignancies for rare disease
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Intellectual disability
- Haematological malignancies cancer susceptibility
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: DOCK8 was added gene: DOCK8 was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Melbourne Genomics Health Alliance Immunology Flagship,Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Immunology Flagship Mode of inheritance for gene: DOCK8 was set to Unknown