Mucopolysaccharideosis, Gaucher, Fabry
Gene: ARSBEnsemblGeneIds (GRCh38): ENSG00000113273
EnsemblGeneIds (GRCh37): ENSG00000113273
OMIM: 611542, Gene2Phenotype
ARSB is in 15 panels
3 reviews
alisdair mcneill (Sheffield childrens hospital)
known gene for lysosomal storage disorderCreated: 1 Jul 2016, 7:56 a.m.
Ellen McDonagh (Genomics England Curator)
Comment when marking as ready: Green gene with green review, and is a confirmed DD gene for this disorder. Mode of inheritance confirmed on G2P and OMIM.
Created: 29 Feb 2016, 5:48 p.m.
Helen Savage (Congenica Ltd)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mucopolysaccharidosis type VI
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Emory Genetics Laboratory
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200
- Mucopolysaccharidosis, Type VI
- Mucopolysaccharidosis Type VI
- MUCOPOLYSACCHARIDOSIS TYPE 6
- OMIM
- 611542
- Clinvar variants
- Variants in ARSB
- Penetrance
- Complete
- Panels with this gene
-
- Undiagnosed metabolic disorders
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Skeletal dysplasia
- Mucopolysaccharideosis, Gaucher, Fabry
- Likely inborn error of metabolism
- Hyperammonaemia
- Paediatric or syndromic cardiomyopathy
- Hydrocephalus
- Mucopolysaccharidosis type VI
- Intellectual disability
- Monogenic hearing loss
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Lysosomal storage disorder
- Fetal anomalies
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 ARSB were set to Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200; Mucopolysaccharidosis, Type VI; Mucopolysaccharidosis Type VI; MUCOPOLYSACCHARIDOSIS TYPE 6
Added New Source
Eik Haraldsdottir (Genomics England)ARSB was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Emory Genetics Laboratory
Set Mode of Inheritance
Eik Haraldsdottir (Genomics England)Model of inheritance for gene ARSB was changed to BIALLELIC, autosomal or pseudoautosomal
Added New Source
Eik Haraldsdottir (Genomics England)ARSB was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Illumina TruGenome Clinical Sequencing Services
Added New Source
Eik Haraldsdottir (Genomics England)ARSB was added to Mucopolysaccharideosis, Gaucher, Fabrypanel. Sources: Radboud University Medical Center, Nijmegen