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GENATLAS PHENOTYPE
last update : 12-05-2010
Symbol FRTS2
Location 5q35.3
Name Fanconi renotubular syndrome 2
Other name(s)
  • characterized by a defect of proximal renal tubular transport and abnormal tubular endocytic function and urinary megalin deficiency
  • Corresponding gene SLC34A1
    Genetic determination
    Function/system disorder kidney and urinary tract
    Type disease
    Remark(s)