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