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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 |
|---|---|---|
| regulation of epithelial cell migration | ||
| response to nutrient | ||
| lysosomal transport |
|
|
| lysosome organization |
|
|
| positive regulation of neuron projection development |
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:0111395 | mucopolysaccharidosis type IIIA | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10159 | osteonecrosis | |
| DOID:10283 | prostate cancer | |
| DOID:10286 | prostate carcinoma | |
| DOID:10581 | metachromatic leukodystrophy | |
| DOID:10588 | adrenoleukodystrophy | |
| DOID:10763 | hypertension | |
| DOID:10825 | essential hypertension | |
| DOID:10908 | hydrocephalus |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000158 | Macroglossia |
| HP:0000238 | Hydrocephalus |
| HP:0000256 | Macrocephaly |
| HP:0000268 | Dolichocephaly |
| HP:0000280 | Coarse facial features |
| HP:0000365 | Hearing impairment |
| HP:0000501 | Glaucoma |
| HP:0000670 | Carious teeth |
| 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 |
