increased circulating potassium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal concentration in the blood of this alkaline metallic element, the most abundant intracellular ion; anomalies in the extracellular (circulating) concentration have important implications for the function of excitable tissues, such as nerve and muscle (Mammalian Phenotype Ontology, MP_0005627)
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25 gene mutations causing the increased circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
ARRB2 arrestin, beta 2
BRE brain and reproductive organ-expressed (TNFRSF1A modulator)
CLN3 ceroid-lipofuscinosis, neuronal 3
CYFIP2 cytoplasmic FMR1 interacting protein 2
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
FPGS folylpolyglutamate synthase
FXYD4 FXYD domain containing ion transport regulator 4
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MYBPC3 myosin binding protein C, cardiac
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
NR3C2 nuclear receptor subfamily 3, group C, member 2
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
POU3F3 POU class 3 homeobox 3
REN renin
RYR1 ryanodine receptor 1 (skeletal)
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SECISBP2 SECIS binding protein 2
TXNIP thioredoxin interacting protein
UMOD uromodulin
WNK4 WNK lysine deficient protein kinase 4
WWOX WW domain containing oxidoreductase
ZBTB20 zinc finger and BTB domain containing 20