Epileptic encephalopathy
Gene: TPP1EnsemblGeneIds (GRCh38): ENSG00000166340
EnsemblGeneIds (GRCh37): ENSG00000166340
OMIM: 607998, Gene2Phenotype
TPP1 is in 18 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)
"TTPI" was submitted by an expert, which is most likely to be this HGNC-approved symbol.Created: 1 Jul 2015, 3:17 p.m.
Details
- Sources
-
- Expert Review Red
- Expert
- OMIM
- 607998
- Clinvar variants
- Variants in TPP1
- Penetrance
- Complete
- Panels with this gene
-
- Lysosomal storage disorder
- Intellectual disability
- Early onset or syndromic epilepsy
- Neuronal ceroid lipofuscinosis type 2
- Neuronal ceroid lipofuscinosis
- Undiagnosed metabolic disorders
- Hyperammonaemia
- Hereditary ataxia
- Fetal anomalies
- Ataxia and cerebellar anomalies - childhood onset
- Retinal disorders
- Likely inborn error of metabolism
- Dystonia, chorea or related movement disorder, childhood onset
- Structural eye disease
- Neurodegenerative disorders, adult onset
- DDG2P
- Hereditary ataxia, adult onset
- Glaucoma (developmental)
History Filter Activity
gel status update
GEL ()The Gel status was updated for this whole panel
Added New Source
Ellen McDonagh (Genomics England Curator)TPP1 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)TPP1 was added to Epileptic encephalopathypanel. Sources: Expert