A mutation in the SLC34A3 gene has been known to cause the
autosomal recessive condition hereditary
hypophosphatemic rickets with
hypercalciuria. This gene is correlated closely with
SLC34A1, an analogue sodium phosphate cotransporter protein. Symptoms include renal phosphate wasting in addition to increase levels of
1,25-dihydroxyvitamin D (yields the hypercalcuria). == See also ==