Mucopolysaccharideosis, Gaucher, Fabry
Gene: NAGLUEnsemblGeneIds (GRCh38): ENSG00000108784
EnsemblGeneIds (GRCh37): ENSG00000108784
OMIM: 609701, Gene2Phenotype
NAGLU is in 20 panels
2 reviews
Ellen McDonagh (Genomics England Curator)
Comment when marking as ready: Green gene, with a green review and is a confirmed gene on G2P for this phenotype. Mode of inheritance confirmed on G2P and OMIM.Created: 29 Feb 2016, 6:07 p.m.
Helen Savage (Congenica Ltd)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mucopolysaccharidosis type IIIB
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- UKGTN
- Emory Genetics Laboratory
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920
- Mucopolysaccharidosis, Type III
- Mucopolysaccharidosis Type IIIB
- Mucopolysaccharidosis Type III
- MUCOPOLYSACCHARIDOSIS TYPE 3B
- OMIM
- 609701
- Clinvar variants
- Variants in NAGLU
- Penetrance
- Complete
- Panels with this gene
-
- Hereditary neuropathy
- DDG2P
- Mucopolysaccharideosis, Gaucher, Fabry
- Intellectual disability
- Hyperammonaemia
- Mucopolysaccharidosis type IIIB
- Adult onset neurodegenerative disorder
- Likely inborn error of metabolism
- Hereditary ataxia with onset in adulthood
- Ataxia and cerebellar anomalies - narrow panel
- Pain syndromes
- Paediatric or syndromic cardiomyopathy
- Hereditary ataxia
- Fetal anomalies
- Paroxysmal central nervous system disorders
- Hereditary neuropathy or pain disorder
- Undiagnosed metabolic disorders
- Skeletal dysplasia
- Lysosomal storage disorder
- Childhood onset dystonia, chorea or related movement disorder
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Phenotypes
Ellen McDonagh (Genomics England Curator)Phenotypes for NAGLU were set to Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920; Mucopolysaccharidosis, Type III; Mucopolysaccharidosis Type IIIB; Mucopolysaccharidosis Type III; MUCOPOLYSACCHARIDOSIS TYPE 3B
Added New Source
Eik Haraldsdottir (Genomics England)NAGLU was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: UKGTN
Added New Source
Eik Haraldsdottir (Genomics England)NAGLU was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Emory Genetics Laboratory
Set Mode of Inheritance
Eik Haraldsdottir (Genomics England)Model of inheritance for gene NAGLU was changed to BIALLELIC, autosomal or pseudoautosomal
Added New Source
Eik Haraldsdottir (Genomics England)NAGLU was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Illumina TruGenome Clinical Sequencing Services
Added New Source
Eik Haraldsdottir (Genomics England)NAGLU was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Radboud University Medical Center, Nijmegen