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arylsulfatase G
Summary
- Gene Symbol
-
- ARSG
- Aliases
-
- KIAA1001
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| sulfur compound metabolic process |
|
|
| lysosome organization |
|
|
| glial cell differentiation |
|
|
| gene expression |
|
|
| homeostasis of number of cells |
|
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region |
|
|
| obsolete extracellular space |
|
|
| lysosome |
|
|
| lysosome |
|
|
| endoplasmic reticulum |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| arylsulfatase activity |
|
|
| arylsulfatase activity |
|
|
| arylsulfatase activity |
|
|
| arylsulfatase activity |
|
|
| hydrolase activity |
|
|
GO Hierarchy
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
| Gene Ontology |
|---|
| hydrolase activity |
| sulfuric ester hydrolase activity |
| InterPro |
|---|
| Alkaline-phosphatase-like, core domain superfamily |
| Sulfatase, N-terminal |
| Sulfatase, conserved site |
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050439 | Usher syndrome |
- The Human Phenotype Ontology
| 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 |
| Disease ID | Disease Name |
|---|---|
| OMIM:618144 |
|
| ORPHA:231183 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP005434
- Gene Name
- arylsulfatase G
