| GENE NAME | STS |
| CHROMOSOME | X |
| ENSEMBL ID | ENSG00000101846 |
| ENTREZ ID | 412 |
| UNIPROT ACCESSION NUMBER | P08842 |
| GO MOLECULAR FUNCTION | sulfuric ester hydrolase activity; steryl-sulfatase activity; hydrolase activity; catalytic activity; arylsulfatase activity; metal ion binding |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-392499; R-HSA-163841; R-HSA-597592; R-HSA-1663150; R-HSA-1430728; R-HSA-1660662; R-HSA-428157; hsa00140; R-HSA-556833 |
| 2 combinations linked to STS | OLI853; OLI907 |
| 2 variants linked to STS | Copy Number Variant deletion on chromosome X of the whole gene in the gene STS; STS:c.770A>G, p.Tyr257Cys |
| 2 diseases linked to STS | Normosmic congenital hypogonadotropic hypogonadism; Kallmann syndrome |