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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
carbohydrate sulfotransferase 11
Summary
- Gene Symbol
-
- CHST11
- Aliases
-
- C4ST
- C4ST1
- C4St-1
- HSA269537
- chondroitin 4-sulfotransferase 1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Carbohydrate metabolism
- Chromosomal rearrangement
- Disease variant
- Dwarfism
- Glycoprotein
- Golgi apparatus
- Reference proteome
- Signal-anchor
- Transferase
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9NPF2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| embryonic viscerocranium morphogenesis | ||
| carbohydrate biosynthetic process |
GO Hierarchy
biological process
metabolic process [inference]
biological regulation [inference]
regulation of biological process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| N-acetylgalactosamine 4-O-sulfotransferase activity | ||
| N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase activity | ||
| sulfotransferase activity | ||
| chondroitin 4-sulfotransferase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
GlycoGene Database (GGDB)
- GGDB ID
- gg036
- Gene Symbol
-
- CHST11
- Reactions
G71793UG
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | XP_235007 | XM_235007 |
| Drosophila melanogaster | NP_608920 | NM_135076 |
| Mus musculus | NP_067414 | NM_021439 |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050469 | Costello syndrome | |
| DOID:0060249 | scoliosis | |
| DOID:0060868 | leukoencephalopathy with vanishing white matter | |
| DOID:1040 | chronic lymphocytic leukemia | |
| DOID:1612 | breast cancer | |
| DOID:162 | cancer | |
| DOID:1703 | Richter's syndrome | |
| DOID:2394 | ovarian cancer | |
| DOID:3459 | breast carcinoma | |
| DOID:3571 | liver cancer |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002938 | Lumbar hyperlordosis |
| HP:0002999 | Patellar dislocation |
| HP:0003388 | Easy fatigability |
| HP:0003502 | Mild short stature |
| HP:0008080 | Hallux varus |
| HP:0009774 | Triangular shaped phalanges of the hand |
| HP:0009778 | Short thumb |
| HP:0009882 | Short distal phalanx of finger |
| HP:0010055 | Broad hallux |
| HP:0010109 | Short hallux |
| Disease ID | Disease Name |
|---|---|
| OMIM:618167 |
|
PubChem Disease
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 105536214 | MANLE09935 | ||
| 101133837 | GORGO05759 | ||
| 100975988 | PANPA10233 | ||
| 467113 | PANTR06757 | ||
| 100457862 | PONAB06180 | ||
| 481299 | CANLF01703 | ||
| 123780888 | URSAM09556 | ||
| 100475790 | AILME16631 | ||
| 101692863 | MUSPF17335 | ||
| 101085731 | FELCA16656 |
