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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
galactosamine (N-acetyl)-6-sulfatase
Summary
- Gene Symbol
-
- GALNS
- Aliases
-
- GALNAC6S
- GAS
- GalN6S
- Morquio syndrome
- N-acetylgalactosamine-6-sulfatase
- chondroitinase
- chondroitinsulfatase
- galactose-6-sulfate sulfatase
- mucopolysaccharidosis type IVA
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Dwarfism
- Glycoprotein
- Hydrolase
- Lysosome
- Metal-binding
- Mucopolysaccharidosis
- Reference proteome
- Signal
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region |
|
|
| lysosomal lumen |
|
|
| extracellular exosome | ||
| azurophil granule lumen |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| N-acetylgalactosamine-4-sulfatase activity |
|
|
| N-acetylgalactosamine-6-sulfatase activity |
|
|
| sulfuric ester hydrolase 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.
KEGG BRITE Database
G77399JK
G71561JP
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0040085 | bacterial sepsis | |
| DOID:0060249 | scoliosis | |
| DOID:0060320 | inguinal hernia | |
| DOID:0060350 | adenine phosphoribosyltransferase deficiency | |
| DOID:0060891 | Parkinson's disease 19A | |
| DOID:0060895 | Parkinson's disease 4 | |
| DOID:0060896 | Parkinson's disease 23 | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080348 | Alzheimer's disease 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000154 | Wide mouth |
| HP:0000280 | Coarse facial features |
| HP:0000303 | Mandibular prognathia |
| HP:0000365 | Hearing impairment |
| HP:0000470 | Short neck |
| HP:0000670 | Carious teeth |
| HP:0000683 | Grayish enamel |
| HP:0000687 | Widely spaced teeth |
| Disease ID | Disease Name |
|---|---|
| OMIM:253000 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 179194 | WB:WBGene00006309 | ||
| 102351372 | LATCH03438 | ||
| 791159 | ZFIN:ZDB-GENE-070112-1152 | DANRE40801 | |
| 108259597 | ICTPU22148 | ||
| 113575705 | ELEEL14888 | ||
| 115167380 | SALTR83121 | ||
| 115558605 | GADMO11731 | ||
| 101171730 | ORYLA12299 | ||
| 100694056 | ORENI34580 | ||
| 115580638 | SPAAU24450 |
