increased circulating phosphate level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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31 gene mutations causing the increased circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ACVR1B activin A receptor, type IB
ARRB2 arrestin, beta 2
CASR calcium-sensing receptor
COL4A5 collagen, type IV, alpha 5
COX19 COX19 cytochrome c oxidase assembly factor
FAM117B family with sequence similarity 117, member B
FGF23 fibroblast growth factor 23
GALC galactosylceramidase
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GCM2 glial cells missing homolog 2 (Drosophila)
GNAS GNAS complex locus
KL klotho
MCF2L MCF.2 cell line derived transforming sequence-like
MYSM1 Myb-like, SWIRM and MPN domains 1
NPTN neuroplastin
PHOSPHO1 phosphatase, orphan 1
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
PITX3 paired-like homeodomain 3
RPL38 ribosomal protein L38
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SATB2 SATB homeobox 2
SFRP1 secreted frizzled-related protein 1
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SLC38A10 solute carrier family 38, member 10
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TMEM68 transmembrane protein 68
WWOX WW domain containing oxidoreductase
ZNF175 zinc finger protein 175