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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:0001371 | Flexion contracture |
| HP:0001385 | Hip dysplasia |
| HP:0001387 | Joint stiffness |
| HP:0001537 | Umbilical hernia |
| HP:0001638 | Cardiomyopathy |
| HP:0001653 | Mitral regurgitation |
| HP:0001718 | Mitral stenosis |
| HP:0001744 | Splenomegaly |
| HP:0002090 | Pneumonia |
| HP:0002091 | Restrictive ventilatory defect |
| 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 |
|---|---|---|---|
| 118893004 | BALMU06125 | ||
| 100073268 | HORSE08839 | ||
| 102158016 | PIGXX19305 | ||
| 538401 | BOVIN00415 | ||
| 102189402 | CAPHI01234 | ||
| 105985324 | DIPOR07807 | ||
| 11881 | MGI:88075 | MOUSE11850 | |
| 25227 | RGD:2158 | RATNO24366 | |
| 100724077 | CAVPO20745 | ||
| 101582679 | OCTDE24352 |
