abnormal urine phosphate concentration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal phosphate concentration in the urine. (Human Phenotype Ontology, HP_0012599)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012599
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Genes

24 genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDOB aldolase B, fructose-bisphosphate
ATP7B ATPase, Cu++ transporting, beta polypeptide
CASR calcium-sensing receptor
CLCN5 chloride channel, voltage-sensitive 5
COA5 cytochrome c oxidase assembly factor 5
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX14 COX14 cytochrome c oxidase assembly factor
COX20 COX20 cytochrome c oxidase assembly factor
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
EHHADH enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
FASTKD2 FAST kinase domains 2
FGF23 fibroblast growth factor 23
HRAS Harvey rat sarcoma viral oncogene homolog
INPPL1 inositol polyphosphate phosphatase-like 1
KRAS Kirsten rat sarcoma viral oncogene homolog
OCRL oculocerebrorenal syndrome of Lowe
PET100 PET100 homolog (S. cerevisiae)
PHEX phosphate regulating endopeptidase homolog, X-linked
PTH1R parathyroid hormone 1 receptor
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
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
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I