Epileptic encephalopathy
Gene: GAMTEnsemblGeneIds (GRCh38): ENSG00000130005
EnsemblGeneIds (GRCh37): ENSG00000130005
OMIM: 601240, Gene2Phenotype
GAMT is in 10 panels
4 reviews
Amy McTague (UCL Institute of Child Health)
Natalie Trump (NHS - Great Ormond Street Hospital)
Manju Kurian (UCL-Institute of Child Health)
Richard Scott (North Thames GMC/UCL)
Details
- Sources
-
- Expert Review Red
- Expert
- OMIM
- 601240
- Clinvar variants
- Variants in GAMT
- Penetrance
- Complete
- Panels with this gene
-
- Early onset dystonia
- Neurodegenerative disorders, adult onset
- Fetal anomalies
- Dystonia, chorea or related movement disorder, adult onset
- Undiagnosed metabolic disorders
- Early onset or syndromic epilepsy
- DDG2P
- Dystonia, chorea or related movement disorder, childhood onset
- Intellectual disability
- Likely inborn error of metabolism
History Filter Activity
gel status update
GEL ()The Gel status was updated for this whole panel
Added New Source
Ellen McDonagh (Genomics England Curator)GAMT was added to Epileptic encephalopathypanel. Source: Expert Review Red
gel status update
GEL ()The Gel status was updated for this whole panel
Added New Source
Ellen McDonagh (Genomics England Curator)GAMT was added to Epileptic encephalopathypanel. Sources: Expert