This Panel is marked as Deleted
Immunological disorders Victorian Clinical Genetics Services
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
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 102582
- Clinvar variants
- Variants in STAT3
- Penetrance
- None
- Panels with this gene
-
- Haematological malignancies cancer susceptibility
- Familial pulmonary fibrosis
- Neonatal diabetes
- COVID-19 research
- Fetal anomalies
- Monogenic diabetes
- Severe multi-system atopic disease with high IgE
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Haematological malignancies for rare disease
- Familial diabetes
- Multi-organ autoimmune diabetes
- Rare genetic inflammatory skin disorders
- Gastrointestinal epithelial barrier disorders
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Familial Meniere Disease
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)STAT3 was added to Immunological disorders Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)STAT3 was created by Sarah Leigh