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MIRAGE
arylsulfatase A
Summary
- Gene Symbol
-
- ARSA
- Aliases
-
- ASA
- metachromatic leucodystrophy
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Hydrolase
- Ichthyosis
- Lipid metabolism
- Lysosome
- Metachromatic leukodystrophy
- Metal-binding
- Proteomics identification
- Reference proteome
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| P15289 |
|
| B4DVI5 |
|
| A0A0C4DFZ2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| lipid metabolic process |
|
|
| autophagy |
|
|
| binding of sperm to zona pellucida |
|
|
| response to nutrient |
|
|
| response to pH |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| acrosomal vesicle |
|
|
| extracellular region |
|
|
| obsolete extracellular space |
|
|
| lysosome |
|
|
| lysosome |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| arylsulfatase activity |
|
|
| arylsulfatase activity |
|
|
| arylsulfatase activity |
|
|
| cerebroside-sulfatase activity |
|
|
| cerebroside-sulfatase activity |
|
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- arylsulfatase I
- Functional Category
-
- E: Amino acid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| hydrolase activity |
| sulfuric ester hydrolase activity |
| InterPro |
|---|
| Alkaline-phosphatase-like, core domain superfamily |
| Sulfatase, N-terminal |
| Sulfatase, conserved site |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10581 | metachromatic leukodystrophy |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000020 | Urinary incontinence |
| HP:0000648 | Optic atrophy |
| HP:0000649 | Abnormality of visual evoked potentials |
| HP:0000712 | Emotional lability |
| HP:0000716 | Depression |
| HP:0000726 | Dementia |
| HP:0000736 | Short attention span |
| HP:0000738 | Hallucinations |
| HP:0000746 | Delusion |
| Disease ID | Disease Name |
|---|---|
| OMIM:250100 |
|
| ORPHA:309263 |
|
| ORPHA:309256 |
|
| ORPHA:309271 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002799
- Gene Name
- arylsulfatase A
