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. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Zhao, Wang, Li, Dong, Wu: "Arylsulfatase B Mediates the Sulfonation-Transport Interplay in Human Embryonic Kidney 293 Cells Overexpressing Sulfotransferase 1A3." in: Drug metabolism and disposition: the biological fate of chemicals, Vol. 44, Issue 9, pp. 1441-9, (2018) (PubMed).
Bhattacharyya, Look, Tobacman: "Increased arylsulfatase B activity in cystic fibrosis cells following correction of CFTR." in: Clinica chimica acta; international journal of clinical chemistry, Vol. 380, Issue 1-2, pp. 122-7, (2007) (PubMed).
Aliases for Arylsulfatase B 抗体
arylsulfatase B (ARSB) 抗体 arylsulfatase B (Arsb) 抗体 arylsulfatase (RB348) 抗体 arylsulfatase B (LOC5566067) 抗体 arylsulfatase b (CpipJ_CPIJ011047) 抗体 arylsulfatase B (VDBG_03275) 抗体 arylsulfatase B (arsb) 抗体 arylsulfatase B (LOC5579667) 抗体 1110007C02Rik 抗体 AI480648 抗体 ARSB 抗体 As-1 抗体 As-1r 抗体 As-1s 抗体 As-1t 抗体 As1 抗体 As1-r 抗体 As1-s 抗体 As1-t 抗体 ASB 抗体 Asr-1 抗体 Ast-1 抗体 G4S 抗体 MPS6 抗体