UniProt | Protein Name |
---|---|
O00204 |
|
GO Term | Evidence Code | PMID |
---|---|---|
sulfation | ||
negative regulation of cell population proliferation | ||
3'-phosphoadenosine 5'-phosphosulfate metabolic process | ||
cholesterol metabolic process | ||
steroid metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
steroid sulfotransferase activity | ||
small molecule binding | ||
cholesterol binding | ||
cholesterol sulfotransferase activity | ||
sulfotransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
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 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000083 | Renal insufficiency |
HP:0000164 | Abnormality of the dentition |
HP:0000232 | Everted lower lip vermilion |
HP:0000365 | Hearing impairment |
HP:0000389 | Chronic otitis media |
HP:0000491 | Keratitis |
HP:0000656 | Ectropion |
HP:0000958 | Dry skin |
HP:0000962 | Hyperkeratosis |
Disease ID | Disease Name |
---|---|
OMIM:617571 |
|
ORPHA:79394 |
|
ORPHA:313 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103743615 | NANGA12366 | ||
115618821 | STRHB02156 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024