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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:0000007 | Autosomal recessive inheritance |
| HP:0000767 | Pectus excavatum |
| HP:0001049 | Absent dorsal skin creases over affected joints |
| HP:0001156 | Brachydactyly |
| HP:0001181 | Adducted thumb |
| HP:0001387 | Joint stiffness |
| HP:0001845 | Overlapping toe |
| HP:0001852 | Sandal gap |
| HP:0002650 | Scoliosis |
| HP:0002829 | Arthralgia |
| Disease ID | Disease Name |
|---|---|
| OMIM:618167 |
|
PubChem Disease
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 326156 | FB:FBgn0032618 | ||
| 103179823 | CALMI18796 | ||
| 404232 | ZFIN:ZDB-GENE-040315-1 | DANRE33150 | |
| 103021340 | ASTMX16165 | ||
| 108279776 | ICTPU12899 | ||
| 113584401 | ELEEL32743 | ||
| 115180019 | SALTR56075 | ||
| 115595618 | SPAAU49105 | ||
| 108711031 | Xenbase:XB-GENE-17339976 | ||
| 108713201 | Xenbase:XB-GENE-17339977 |
