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SLC45A2 (solute carrier family 45 member 2)

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اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • Contributors:
      University of Calcutta, Department of Genetics, 35, Ballygunge Circular Road, Kolkata - 700 019, India (MS, TD); ATGC Diagnostics Private Limited, Kolkata, India, (KR)
    • بيانات النشر:
      ARMGHM - Atlas Génétique des Cancers
    • الموضوع:
      2019
    • Collection:
      I-Revues (E-Journals, INIST-CNRS)
    • نبذة مختصرة :
      SLC45A2 gene, having a chromosomal location 5p13.2, encodes a membrane associated transporter protein (MATP). MATP is a transmembrane protein. It is present in the melanosomal membrane in the melanocytes. It maintains the osmotic potential by regulating the pH of the melanosomal lumen. Defects in the SLC45A2 gene causes oculocutaneous albinism type IV; OCA IV
    • ISSN:
      1768-3262
    • Relation:
      Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Genes/SLC45A2ID41306ch5p13.html; Mainak, Sengupta; Tithi, Dutta; Kunal, Ray. SLC45A2 (solute carrier family 45 member 2). Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 07, p. 187-189; http://hdl.handle.net/2042/70469; https://doi.org/10.4267/2042/70469
    • الرقم المعرف:
      10.4267/2042/70469
    • Rights:
      Open access resource - terms and conditions : http://irevues.inist.fr/utilisation
    • الرقم المعرف:
      edsbas.FE049F69