Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
Guidelines
MIRAGE
arylsulfatase G

Summary
Gene Symbol
  • ARSG
Aliases
  • KIAA1001
Organism
Homo sapiens (human)
NCBI Gene
22901
HGNC
24102
KEGG Gene ID
hsa:22901
PubChem
22901
Alliance of Genome Resources
Annotation
Keyword
  • Calcium
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Hydrolase
  • Lysosome
  • Metal-binding
  • Reference proteome
  • Retinitis pigmentosa
  • Signal
  • Usher syndrome
Proteins
Displaying 1 entry
UniProt Protein Name
Q96EG1
  • N-sulfoglucosamine-3-sulfatase
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 7 in total
GO Term Evidence Code PMID
sulfur compound metabolic process
lysosome organization
glial cell differentiation
gene expression
homeostasis of number of cells
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
arylsulfatase I
Functional Category
  • E: Amino acid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Displaying all 2 entries
Gene Ontology
hydrolase activity
sulfuric ester hydrolase activity
Displaying all 3 entries
InterPro
Alkaline-phosphatase-like, core domain superfamily
Sulfatase, N-terminal
Sulfatase, conserved site
KEGG BRITE Database
Orthology
K12381
Name
arylsulfatase G [EC:3.1.6.-]
References
Rhea

RHEA:17261

an aryl sulfate + H2O
H+ + sulfate + a phenol
Enzyme
PMID
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0050439 Usher syndrome
The Human Phenotype Ontology
Displaying entries 1 - 10 of 24 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000375 Abnormal cochlea morphology
HP:0000407 Sensorineural hearing impairment
HP:0000408 Progressive sensorineural hearing impairment
HP:0000483 Astigmatism
HP:0000512 Abnormal electroretinogram
HP:0000518 Cataract
HP:0000546 Retinal degeneration
HP:0000572 Visual loss
HP:0000575 Scotoma
Displaying all 2 entries
Disease ID Disease Name
ORPHA:231183
  • Usher syndrome type 3
  • retinitis pigmentosa-deafness syndrome
OMIM:618144
  • Usher syndrome, type 4
PubChem Disease
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP005434
Gene Name
arylsulfatase G
Ortholog
Displaying entries 31 - 40 of 79 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
101594358 JACJA06487
101675284 MUSPF15065
101931439 CHRPI03625
101959528 ICTTR03032
102027638 CHILA17726
102179519 CAPHI11509
102363561 LATCH16270
102436364 MYOLU07033
102449875 PELSI10311
103175517 CALMI08194
About Release Notes Help Feedback
International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.4.0

Last updated: December 8, 2025