This Panel is marked as Retired
Epilepsy Plus
Gene: FOXG1
FOXG1 (forkhead box G1)
EnsemblGeneIds (GRCh38): ENSG00000176165
EnsemblGeneIds (GRCh37): ENSG00000176165
OMIM: 164874, Gene2Phenotype
FOXG1 is in 10 panels
EnsemblGeneIds (GRCh38): ENSG00000176165
EnsemblGeneIds (GRCh37): ENSG00000176165
OMIM: 164874, Gene2Phenotype
FOXG1 is in 10 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- UKGTN
- Expert
- Phenotypes
-
- Rett syndrome, congenital variant
- OMIM
- 164874
- Clinvar variants
- Variants in FOXG1
- Penetrance
- Complete
- Publications
-
- PMID: 21441262
- Panels with this gene
-
- Monogenic hearing loss
- Early onset dystonia
- Intellectual disability
- Early onset or syndromic epilepsy
- Adult onset dystonia, chorea or related movement disorder
- Severe microcephaly
- Adult onset neurodegenerative disorder
- Fetal anomalies
- DDG2P
- Childhood onset dystonia, chorea or related movement disorder
History Filter Activity
8 Sep 2016, Gel status: 0
Created
Ellen McDonagh (Genomics England Curator)FOXG1 was created by ellenmcdonagh
8 Sep 2016, Gel status: 4
Added New Source
Ellen McDonagh (Genomics England Curator)FOXG1 was added to Epilepsy Pluspanel. Sources: UKGTN,Expert,Expert Review Green