increased urine phosphate level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002901
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Genes

11 gene mutations causing the increased urine phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLCN5 chloride channel, voltage-sensitive 5
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
GPRC6A G protein-coupled receptor, class C, group 6, member A
HNF1A HNF1 homeobox A
KCNK1 potassium channel, two pore domain subfamily K, member 1
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SLC9A3R1 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1
TRPV5 transient receptor potential cation channel, subfamily V, member 5
UMOD uromodulin