415
n/a
ENSG00000157399
P51690
NM_000047NM_001282628NM_001282631NM_001369079NM_001369080
NP_001269557.1NP_001269560.1
Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene.[3]
Arylsulfatase L is a member of the arylsulfatase subfamily of sulfatase enzymes that catalyze the hydrolysis of sulfate esters. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix.[4]
Deficiencies in ARSL are associated with X-linked recessive chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development.[5]
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.
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