Arylsulfatase L

ARSL
Identifiers
Aliases	ARSL, ASE, CDPX, CDPX1, CDPXR, arylsulfatase E (chondrodysplasia punctata 1), arylsulfatase E, arylsulfatase L, ARSE
External IDs	OMIM: 300180; HomoloGene: 55428; GeneCards: ARSL; OMA:ARSL - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	2,968,475 bp
RNA expression pattern
	Top expressed in
	body of pancreas; ; liver; ; right lobe of liver; ; gonad; ; mucosa of transverse colon; ; human kidney; ; rectum; ; islet of Langerhans; ; mucosa of sigmoid colon; ; mucosa of ileum;
	n/a
	More reference expression data
	n/a
Gene ontology
Molecular function	sulfuric ester hydrolase activity; catalytic activity; hydrolase activity; arylsulfatase activity; metal ion binding;
Cellular component	Golgi stack; endoplasmic reticulum lumen; extracellular exosome; Golgi apparatus; membrane; integral component of membrane;
Biological process	post-translational protein modification; skeletal system development; metabolism; glycosphingolipid metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	415
	n/a
	ENSG00000157399
	n/a
	P51690
	n/a
	NM_000047; NM_001282628; NM_001282631; NM_001369079; NM_001369080
	n/a
NP_000038; NP_001269557; NP_001269560; NP_001356008; NP_001356009;
	NP_001269557.1; NP_001269560.1
	n/a
	Wikidata
View/Edit Human

Arylsulfatase L is an enzyme that, in humans, is encoded by the ARSL gene.^[3]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000157399 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Franco B, Meroni G, Parenti G, Levilliers J, Bernard L, Gebbia M, Cox L, Maroteaux P, Sheffield L, Rappold GA (April 1995). "A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy". Cell. 81 (1): 15–25. doi:10.1016/0092-8674(95)90367-4. PMID 7720070.