Monogenic diabetes
Gene: FOXC2EnsemblGeneIds (GRCh38): ENSG00000176692
EnsemblGeneIds (GRCh37): ENSG00000176692
OMIM: 602402, Gene2Phenotype
FOXC2 is in 13 panels
1 review
Ivone Leong (Genomics England Curator)
Gene changed to grey status after consultation with Professor Sian Ellard (South West GLH) that this gene is not appropriate for the panel.Created: 25 Jan 2019, 11:49 a.m.
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Removed
- Phenotypes
-
- Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400
- Lymphedema-distichiasis syndrome, 153400
- Tags
- OMIM
- 602402
- Clinvar variants
- Variants in FOXC2
- Penetrance
- None
- Panels with this gene
-
- Unexplained young onset end-stage renal disease - additional genes
- Rare genetic inflammatory skin disorders
- Vascular skin disorders
- Unexplained kidney failure in young people
- DDG2P
- Monogenic diabetes
- Fetal anomalies
- Clefting
- Fetal hydrops
- Primary lymphoedema
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Intellectual disability
- CAKUT
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: FOXC2.
Panel promoted to version 1.0
Ivone Leong (Genomics England Curator)Ivone Leong: Gene changed to grey status af
Added New Source, Status Update
Ivone Leong (Genomics England Curator)Source Expert Review Removed was added to FOXC2. Rating Changed from Red List (low evidence) to No List (delete)
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: FOXC2 was added gene: FOXC2 was added to Monogenic diabetes. Sources: Expert Review Red Mode of inheritance for gene: FOXC2 was set to Unknown Phenotypes for gene: FOXC2 were set to Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, 153400; Lymphedema-distichiasis syndrome, 153400