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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:2256 | osteochondrodysplasia | |
| DOID:2348 | arteriosclerotic cardiovascular disease | |
| DOID:2349 | arteriosclerosis | |
| DOID:2468 | psychotic disorder | |
| DOID:2581 | chondrodysplasia punctata | |
| DOID:2752 | glycogen storage disease II | |
| DOID:3083 | chronic obstructive pulmonary disease | |
| DOID:319 | spinal cord disease | |
| DOID:3211 | lysosomal storage disease | |
| DOID:331 | central nervous system disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002092 | Pulmonary arterial hypertension |
| HP:0002240 | Hepatomegaly |
| HP:0002318 | Cervical myelopathy |
| HP:0002656 | Epiphyseal dysplasia |
| HP:0002751 | Kyphoscoliosis |
| HP:0002788 | Recurrent upper respiratory tract infections |
| HP:0002829 | Arthralgia |
| HP:0002857 | Genu valgum |
| HP:0002866 | Hypoplastic iliac wing |
| HP:0002869 | Flared iliac wing |
| 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 |
|---|---|---|---|
| 183778 | WB:WBGene00006310 | ||
| 39991 | FB:FBgn0036765 | ||
| 39994 | FB:FBgn0036768 | ||
| 317903 | FB:FBgn0052191 | ||
| 100187202 | CIOIN13273 | ||
| 103177857 | CALMI13773 | ||
| 102353782 | LATCH15956 | ||
| 102689449 | LEPOC06950 | ||
| 110438237 | ZFIN:ZDB-GENE-111123-2 | ||
| 108279373 | ICTPU11819 |
