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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
arylsulfatase B
Summary
- Gene Symbol
-
- ARSB
- Aliases
-
- ASB
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Hydrolase
- Ichthyosis
- Lysosome
- Metachromatic leukodystrophy
- Metal-binding
- Mucopolysaccharidosis
- Reference proteome
- Signal
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| response to estrogen | ||
| autophagy | ||
| response to methylmercury | ||
| colon epithelial cell migration | ||
| response to pH |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen |
|
|
| extracellular region |
|
|
| cell surface | ||
| lysosomal lumen |
|
|
| ficolin-1-rich granule lumen |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| N-acetylgalactosamine-4-sulfatase activity | ||
| metal ion binding | ||
| arylsulfatase activity |
|
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:11328 | schizophreniform disorder | |
| DOID:11984 | hypertrophic cardiomyopathy | |
| DOID:12798 | mucopolysaccharidosis | |
| DOID:12799 | mucopolysaccharidosis II | |
| DOID:12800 | mucopolysaccharidosis VI | |
| DOID:12801 | mucopolysaccharidosis III | |
| DOID:12802 | mucopolysaccharidosis I | |
| DOID:12804 | mucopolysaccharidosis IV | |
| DOID:12932 | endomyocardial fibrosis | |
| DOID:14159 | obstructive hydrocephalus |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000684 | Delayed eruption of teeth |
| HP:0000768 | Pectus carinatum |
| HP:0000884 | Prominent sternum |
| HP:0000885 | Broad ribs |
| HP:0000943 | Dysostosis multiplex |
| HP:0001007 | Hirsutism |
| HP:0001072 | Thickened skin |
| HP:0001171 | Split hand |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| Disease ID | Disease Name |
|---|---|
| OMIM:253200 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115592152 | SPAAU33099 | ||
| 108717994 | Xenbase:XB-GENE-6486738 | ||
| 100493013 | Xenbase:XB-GENE-962085 | ||
| 101938081 | CHRPI23920 | ||
| 109307999 | CROPO12566 | ||
| 103819543 | SERCA14291 | ||
| 100088121 | ORNAN12375 | ||
| 100393734 | CALJA27507 | ||
| 100394090 | CALJA27507 | ||
| 105599169 | CERAT07049 |
