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Gene : STS Homo sapiens

Name  ? steroid sulfatase Cytological Location  Xp22.31
Brief Description  steroid sulfatase
description  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]
  • synonyms:
  • ARSC,
  • XLI,
  • arylsulfatase C,
  • ARSC1,
  • steryl-sulfatase,
  • ARSC1,
  • ES,
  • steroid sulfatase (microsomal), isozyme S,
  • M16505,
  • steroid sulfatase (microsomal), arylsulfatase C, isozyme S,
  • SSDD,
  • ARSC,
  • NM_000351,
  • STS,
  • HGNC:11425,
  • uc004cry.5,
  • OTTHUMG00000021102,
  • ASC
  • identifiers:
  • 412,
  • ENSG00000101846,
  • STS

Genome feature

Region: gene ? Length: 207392  
Location: X:7147252-7354643 Cyto location: Xp22.31


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Proteins

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Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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Other

2011 SN Ps

5 Cross References

19 Data Sets

10 Homologues

0 Located Features

90 Rna Seq Results