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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:0050700 | cardiomyopathy | |
| DOID:0060215 | Balo concentric sclerosis | |
| DOID:0060222 | Scheie syndrome | |
| DOID:0060320 | inguinal hernia | |
| DOID:0060321 | umbilical hernia | |
| DOID:0060327 | omphalocele | |
| DOID:0060357 | chylomicron retention disease | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0111390 | mucopolysaccharidosis Ih | |
| DOID:0111391 | mucopolysaccharidosis IVA |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002938 | Lumbar hyperlordosis |
| HP:0003016 | Metaphyseal widening |
| HP:0003025 | Metaphyseal irregularity |
| HP:0003274 | Hypoplastic acetabulae |
| HP:0003300 | Ovoid vertebral bodies |
| HP:0003311 | Hypoplasia of the odontoid process |
| HP:0003521 | Disproportionate short-trunk short stature |
| HP:0003593 | Infantile onset |
| HP:0004322 | Short stature |
| HP:0005180 | Tricuspid regurgitation |
| 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 |
|---|---|---|---|
| 101879959 | MELUD16362 | ||
| 100032622 | MONDO18033 | ||
| 102445150 | PELSI13307 | ||
| 100564703 | ANOCA02102 | ||
| 107093772 | CYPVA18398 | ||
| 113899711 | BOBOX21474 | ||
| 100944911 | OTOGA15270 | ||
| 112162825 | ORYME18556 | ||
| 101061832 | TAKRU45194 | ||
| 102799236 | NEOBR16958 |
