This Panel is marked as Deleted
Cholestasis Victorian Clinical Genetics Services
Gene: GBA
GBA (glucosylceramidase beta)
EnsemblGeneIds (GRCh38): ENSG00000177628
EnsemblGeneIds (GRCh37): ENSG00000177628
OMIM: 606463, Gene2Phenotype
GBA is in 25 panels
EnsemblGeneIds (GRCh38): ENSG00000177628
EnsemblGeneIds (GRCh37): ENSG00000177628
OMIM: 606463, Gene2Phenotype
GBA is in 25 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 606463
- Clinvar variants
- Variants in GBA
- Penetrance
- None
- Panels with this gene
-
- Haematological malignancies cancer susceptibility
- Intellectual disability
- Familial pulmonary fibrosis
- Early onset or syndromic epilepsy
- DDG2P
- Undiagnosed metabolic disorders
- Mucopolysaccharideosis, Gaucher, Fabry
- Childhood onset dystonia, chorea or related movement disorder
- Hyperammonaemia
- Fetal hydrops
- Lysosomal storage disorder
- Cholestasis
- Haematological malignancies for rare disease
- Adult onset neurodegenerative disorder
- Early onset dementia (encompassing fronto-temporal dementia and prion disease)
- Iron metabolism disorders - NOT common HFE mutations
- Gaucher disease
- Bleeding and platelet disorders
- Inherited bleeding disorders
- Neonatal cholestasis
- Likely inborn error of metabolism
- Parkinson Disease and Complex Parkinsonism
- Arthrogryposis
- Adult onset dystonia, chorea or related movement disorder
- Fetal anomalies
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)GBA was added to Cholestasis Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)GBA was created by Sarah Leigh