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Description for Protein KCNJ12

potassium inwardly-rectifying channel, subfamily J, member 12
17 total interacting proteins; 10 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 0/0)
(Not detected in platelets)
Summary:
This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • TM: Transmembrane domain

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    None Available
    KEGG - Orthology:
    K05005
    KEGG - Pathway(s):
    None Available
    Nomenclature / Alternative Names:
    Potassium inwardly rectifying channel subfamily J inhibitor 1; ATP sensitive inward rectifier potassium channel 12; Inward rectifier K+ channel Kir2.2; IRK2; IRK; KCNJN1; Kir2.2; Kir2.2v
    Approved Symbol:
    KCNJ12
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 5
    Human (de-) phosphorylation sites: 5; 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):

  • Dofetilide(db)


    Associated Genetic Diseases:

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

    HPRD: 09083 Entrez Gene ID: 3768 OMIM ID: 602323 Swissprot Accession: Q14500