Familial Meniere Disease
Gene: FOXP3
FOXP3 (forkhead box P3)
EnsemblGeneIds (GRCh38): ENSG00000049768
EnsemblGeneIds (GRCh37): ENSG00000049768
OMIM: 300292, Gene2Phenotype
FOXP3 is in 16 panels
EnsemblGeneIds (GRCh38): ENSG00000049768
EnsemblGeneIds (GRCh37): ENSG00000049768
OMIM: 300292, Gene2Phenotype
FOXP3 is in 16 panels
0 reviews
Details
- Sources
-
- Literature
- OMIM
- 300292
- Clinvar variants
- Variants in FOXP3
- Penetrance
- None
- Publications
- Panels with this gene
-
- Gastrointestinal epithelial barrier disorders
- Fetal anomalies
- Neonatal diabetes
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Familial Meniere Disease
- IPEX - Immunodysregulation Polyendocrinopathy and Enteropathy, X-Linked
- Monogenic diabetes
- Intellectual disability
- DDG2P
- COVID-19 research
- Intestinal failure or congenital diarrhoea
- Fetal hydrops
- Familial diabetes
- Multi-organ autoimmune diabetes
History Filter Activity
27 Mar 2018, Gel status: 1
Panel promoted to version 1.0
Eleanor Williams (Genomics England Curator)External reviews collated. Internal clinical input. Ready for version 1.
17 Jan 2018, Gel status: 1
Added New Source
Eleanor Williams (Genomics England Curator)FOXP3 was added to Familial Meniere Disease panel. Sources: Literature
17 Jan 2018, Gel status: 1
Created
Eleanor Williams (Genomics England Curator)FOXP3 was created by Eleanor Williams