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
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:2351 | iron metabolism disease | |
| DOID:2352 | hemochromatosis | |
| DOID:2468 | psychotic disorder | |
| DOID:2921 | glomerulonephritis | |
| DOID:299 | adenocarcinoma | |
| DOID:3083 | chronic obstructive pulmonary disease | |
| DOID:3211 | lysosomal storage disease | |
| DOID:3322 | GM1 gangliosidosis | |
| DOID:3385 | bacterial vaginosis | |
| DOID:3459 | breast carcinoma |
- 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 |
|---|---|---|---|
| 495239 | Xenbase:XB-GENE-1000594 | ||
| 100485376 | Xenbase:XB-GENE-1000591 | ||
| 101934226 | CHRPI07654 | ||
| 109310712 | CROPO16657 | ||
| 103816759 | SERCA10024 | ||
| 100089863 | ORNAN02091 | ||
| 100389028 | CALJA21839 | ||
| 105588730 | CERAT00745 | ||
| 697715 | MACMU27095 | ||
| 697850 | MACMU27095 |
