This Panel is marked as Deleted
Immunological disorders_SuperPanel_PanelAppAustralia
Gene: STAT3
STAT3 (signal transducer and activator of transcription 3)
EnsemblGeneIds (GRCh38): ENSG00000168610
EnsemblGeneIds (GRCh37): ENSG00000168610
OMIM: 102582, Gene2Phenotype
STAT3 is in 17 panels
EnsemblGeneIds (GRCh38): ENSG00000168610
EnsemblGeneIds (GRCh37): ENSG00000168610
OMIM: 102582, Gene2Phenotype
STAT3 is in 17 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Melbourne Genomics Health Alliance Immunology Flagship
- OMIM
- 102582
- Clinvar variants
- Variants in STAT3
- Penetrance
- None
- Panels with this gene
-
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Rare genetic inflammatory skin disorders
- Familial Meniere Disease
- Haematological malignancies cancer susceptibility
- Neonatal diabetes
- Familial pulmonary fibrosis
- COVID-19 research
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Severe multi-system atopic disease with high IgE
- Monogenic diabetes
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Haematological malignancies for rare disease
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Familial diabetes
- Multi-organ autoimmune diabetes
- Fetal anomalies
- Gastrointestinal epithelial barrier disorders
History Filter Activity
7 Apr 2020, Gel status: 3
Created, Added New Source, Set mode of inheritance
Rebecca Foulger (Genomics England curator)gene: STAT3 was added gene: STAT3 was added to Immunological disorders_SuperPanel_PanelAppAustralia. Sources: Melbourne Genomics Health Alliance Immunology Flagship,Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: STAT3 was set to Unknown