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Description for Protein USP9X

ubiquitin specific peptidase 9, X-linked
10 total interacting proteins; 6 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 1/0)
(platelet: 3)
Summary:
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • UCH: Ubiquitin carboxyl-terminal hydrolase

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    3.1.2.15
    KEGG - Orthology:
    K11840
    KEGG - Pathway(s):
    None Available
    Nomenclature / Alternative Names:
    Fat facets protein related, X-linked; Deubiquitinating enzyme FAF-X; Ubiquitin-specific processing protease FAF-X; Ubiquitin thiolesterase FAF-X; USP9; Fam; DFFRX; Ubiquitin-specific protease 9, X chromosome; EC 3.1.2.15; Ubiquitin specific protease 9, X-linked isoform 1; Ubiquitin specific protease 9, X-linked isoform 2; Ubiquitin specific protease 9, X-linked isoform 3; Ubiquitin specific protease 9, X-linked isoform 4
    Approved Symbol:
    USP9X
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 34
    Human (de-) phosphorylation sites: 34; No platelet phosphorylation sites

    Phosphorylation Targets:
    Total phosphorylation targets: 0
    Human phosphorylation targets: 0;Predicted platelet targets: 0
    Protein Characteristics:
    Isoform-specific Information
    Icon DrugsAssociated Drugs (DrugBank Accession):

    None Available


    Associated Genetic Diseases:

    None Available
    Predicted Transmembrane Domains:
  • Isoform 4 : 0
  • Isoform 3 : 0
  • Isoform 2 : 0
  • Isoform 1 : 0
  • Additional Identifiers:

    HPRD: 02091 Entrez Gene ID: 8239 OMIM ID: 300072 Swissprot Accession: Q6P468Q93008Q86X58