renal phosphate wasting Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description High urine phosphate in the presence of hypophosphatemia. (Human Phenotype Ontology, HP_0000117)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000117
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Genes

7 genes associated with the renal phosphate wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLCN5 chloride channel, voltage-sensitive 5
FGF23 fibroblast growth factor 23
INPPL1 inositol polyphosphate phosphatase-like 1
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1