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Gene Symbol |
STS |
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Aliases |
ARSC, ARSC1, ASC, ES, SSDD, XLI |
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Entrez Gene ID |
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Gene Name |
Steroid sulfatase |
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Chromosomal Location |
Xp22.31 |
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HGNC ID |
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Summary |
This gene encodes a multi-pass membrane protein that is localized to the endoplasmic reticulum. It belongs to the sulfatase family and hydrolyzes several 3-beta-hydroxysteroid sulfates, which serve as metabolic precursors for estrogens, androgens, and cholesterol. Mutations in this gene are associated with X-linked ichthyosis (XLI). Alternatively spliced transcript variants resulting from the use of different promoters have been described for this gene (PMID:17601726). [provided by RefSeq, Mar 2016]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Steryl-sulfatase, arylsulfatase C, estrone sulfatase, steroid sulfatase (microsomal), isozyme S, steryl-sulfate sulfohydrolase |
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Function |
Catalyzes the conversion of sulfated steroid precursors, such as dehydroepiandrosterone sulfate (DHEA-S) and estrone sulfate to the free steroid. |
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UniProt |
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PDB |
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Pfam |
Pfam Accession |
Pfam ID |
PF00884 |
Sulfatase |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000216492 |
P10645 |
P10645 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Ichthyosis |
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Digestive System Diseases |
Hepatitis, Alcoholic |
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Fatty Liver |
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Endocrine System Diseases |
PCOS |
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Immune System Diseases |
Rheumatoid Arthritis |
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Nutritional and Metabolic Diseases |
Ichthyosis |
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Obesity |
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Psychiatric/Brain disorders |
Minimal Brain Dysfunction |
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Attention Deficit Disorder |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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P450 aromatase, estrogen sulfotransferase (EST) and 17beta-hydroxysteroid dehydrogenase (17beta-HSD) |
Steroid metabolism |
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Related
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The relationship between the activities of STS and EST was lower in PCOSE and HPCOSE (p<0.05) versus CE. |
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