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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
sulfotransferase family 2B member 1
Summary
- Gene Symbol
-
- SULT2B1
- Aliases
-
- HSST2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cytoplasm
- Disease variant
- Ichthyosis
- Microsome
- Nucleus
- Phosphoprotein
- Reference proteome
- Steroid metabolism
- Transferase
- Proteins
| UniProt | Protein Name |
|---|---|
| O00204 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| positive regulation of epidermal cell differentiation |
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular metabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
cellular metabolic process [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| steroid sulfotransferase activity | ||
| small molecule binding | ||
| cholesterol binding | ||
| cholesterol sulfotransferase activity | ||
| sulfotransferase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0040085 | bacterial sepsis | |
| DOID:0060655 | autosomal recessive congenital ichthyosis | |
| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | |
| DOID:0060711 | autosomal recessive congenital ichthyosis 3 | |
| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | |
| DOID:0060714 | autosomal recessive congenital ichthyosis 5 | |
| DOID:0060715 | autosomal recessive congenital ichthyosis 6 | |
| DOID:0060716 | autosomal recessive congenital ichthyosis 7 | |
| DOID:0060717 | autosomal recessive congenital ichthyosis 8 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004322 | Short stature |
| HP:0007479 | Congenital nonbullous ichthyosiform erythroderma |
| HP:0008064 | Ichthyosis |
| HP:0008070 | Sparse hair |
| HP:0010783 | Erythema |
| HP:0011039 | Abnormal helix morphology |
| HP:0100543 | Cognitive impairment |
| HP:0100679 | Lack of skin elasticity |
| HP:0100758 | Gangrene |
| HP:0100806 | Sepsis |
| Disease ID | Disease Name |
|---|---|
| OMIM:617571 |
|
| ORPHA:79394 |
|
| ORPHA:313 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002770
- Gene Name
- sulfotransferase family, cytosolic, 2B, member 1
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 190959 | WB:WBGene00013748 | ||
| 37742 | FB:FBgn0034887 | ||
| 37743 | FB:FBgn0265052 | ||
| 41098 | FB:FBgn0037665 | ||
| 338214 | ZFIN:ZDB-GENE-030219-114 | ||
| 777792 | ZFIN:ZDB-GENE-061117-4 | ||
| 777793 | ZFIN:ZDB-GENE-061117-5 | ||
| 432283 | Xenbase:XB-GENE-17336248 | ||
| 100036899 | Xenbase:XB-GENE-5805920 | ||
| 100497264 | Xenbase:XB-GENE-986082 |
