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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
carbohydrate sulfotransferase 6
Summary
- Gene Symbol
-
- CHST6
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Carbohydrate metabolism
- Corneal dystrophy
- Disease variant
- Glycoprotein
- Golgi apparatus
- Reference proteome
- Signal-anchor
- Transferase
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9GZX3 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| sulfur compound metabolic process | ||
| carbohydrate metabolic process | ||
| keratan sulfate biosynthetic process | ||
| N-acetylglucosamine metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| trans-Golgi network | ||
| Golgi apparatus | ||
| Golgi membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| keratan sulfotransferase activity | ||
| N-acetylglucosamine 6-O-sulfotransferase activity |
GlycoGene Database (GGDB)
- GGDB ID
- gg030
- Gene Symbol
-
- CHST6
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | XP_226482 | XM_226482 |
| Mus musculus | NP_064334 | NM_019950 |
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10141 | obsolete asthenopia | |
| DOID:10871 | age related macular degeneration | |
| DOID:11541 | recurrent corneal erosion | |
| DOID:12318 | granular corneal dystrophy | |
| DOID:2007 | degeneration of macula and posterior pole | |
| DOID:2565 | macular corneal dystrophy | |
| DOID:2566 | corneal dystrophy | |
| DOID:4448 | macular degeneration | |
| DOID:9120 | amyloidosis |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000484 | Hyperopic astigmatism |
| HP:0000495 | Recurrent corneal erosions |
| HP:0000531 | Corneal crystals |
| HP:0000613 | Photophobia |
| HP:0001131 | Corneal dystrophy |
| HP:0001141 | Severely reduced visual acuity |
| HP:0001939 | Abnormality of metabolism/homeostasis |
| HP:0003621 | Juvenile onset |
| HP:0007754 | Macular dystrophy |
| Disease ID | Disease Name |
|---|---|
| OMIM:217800 |
|
| ORPHA:98969 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 33913 | FB:FBgn0031826 | ||
| 33914 | FB:FBgn0051637 | ||
| 103175980 | CALMI09082 | ||
| 102356562 | LATCH01571 | ||
| 100170782 | ZFIN:ZDB-GENE-060810-74 | DANRE26836 | |
| 103042977 | ASTMX21971 | ||
| 108268591 | ICTPU33514 | ||
| 113590900 | ELEEL45827 | ||
| 115151880 | SALTR114852 | ||
| 115550882 | GADMO60672 |
