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
- Fetal anomalies
- Neuronal ceroid lipofuscinosis type 2
- Ataxia and cerebellar anomalies - narrow panel
- Retinal disorders
- Likely inborn error of metabolism
- Neuronal ceroid lipofuscinosis
- Undiagnosed metabolic disorders
- Hyperammonaemia
- Hereditary ataxia with onset in adulthood
- Structural eye disease
- Adult onset neurodegenerative disorder
- Childhood onset dystonia, chorea or related movement disorder
- Early onset or syndromic epilepsy
- DDG2P
- Hereditary ataxia
- 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