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