Epileptic encephalopathy
Gene: GATMEnsemblGeneIds (GRCh38): ENSG00000171766
EnsemblGeneIds (GRCh37): ENSG00000171766
OMIM: 602360, Gene2Phenotype
GATM is in 11 panels
5 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)
Ellen McDonagh (Genomics England Curator)
"AGAT" was submitted by an expert, which is most likely to be this HGNC-approved symbol.Created: 1 Jul 2015, 3:16 p.m.
Details
- Sources
-
- Expert Review Red
- Expert
- OMIM
- 602360
- Clinvar variants
- Variants in GATM
- Penetrance
- Complete
- Panels with this gene
-
- Intellectual disability
- Fetal anomalies
- Childhood onset dystonia, chorea or related movement disorder
- Mitochondrial disorders
- Likely inborn error of metabolism
- Early onset or syndromic epilepsy
- Tubulointerstitial kidney disease
- Renal tubulopathies
- Undiagnosed metabolic disorders
- DDG2P
- Possible mitochondrial disorder - nuclear genes
History Filter Activity
gel status update
GEL ()The Gel status was updated for this whole panel
Added New Source
Ellen McDonagh (Genomics England Curator)GATM 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)GATM was added to Epileptic encephalopathypanel. Sources: Expert