Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0005280 | Depressed nasal bridge |
| HP:0007957 | Corneal opacity |
| HP:0008301 | Dermatan sulfate excretion in urine |
| HP:0008432 | Anterior wedging of L1 |
| HP:0010444 | Pulmonary insufficiency |
| HP:0010535 | Sleep apnea |
| HP:0010885 | Avascular necrosis |
| HP:0011410 | Caesarian section |
| HP:0011463 | Childhood onset |
| HP:0011703 | Sinus tachycardia |
| 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 |
