decreased circulating 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:0000198
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Genes

23 gene mutations causing the decreased circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASR calcium-sensing receptor
CSF1 colony stimulating factor 1 (macrophage)
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FAM20C family with sequence similarity 20, member C
FGF23 fibroblast growth factor 23
GCM2 glial cells missing homolog 2 (Drosophila)
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GNAS GNAS complex locus
GPC5 glypican 5
JAK1 Janus kinase 1
KCNK1 potassium channel, two pore domain subfamily K, member 1
MEN1 multiple endocrine neoplasia I
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
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
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
TRPV5 transient receptor potential cation channel, subfamily V, member 5
UMOD uromodulin
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor