(ARSB) arylsulfatase B [Homo sapiens]
Gene
Transcript(s)
Exon(s)
Protein(s)
Gene
 Accession  26141
 Official symbol  ARSB
 Official name  arylsulfatase B
 Gene type  protein-coding
 Organism  Homo sapiens
 Location  chromosome 5 (NC_000005.8) : 78108788...78318114  (-)
 Map  5q11-q13
 Length  209326  nt
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Alternative name(s) and Synynom(s) top
Synonyms MPS6; G4S; ASB
Names OTTHUMP00000135268
N-acetylgalactosamine-4-sulfatase
External Links top
EC_number 3.1.6.1
Ensembl ENSG00000113273
GeneID 411
HGNC 714
HPRD 08358
Comment top
Summary Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Defects in this gene cause Maroteaux-Lamy syndrome. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
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