decreased circulating potassium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less 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_0005628)
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24 gene mutations causing the decreased circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
BSND barttin CLCNK-type chloride channel accessory beta subunit
CASQ2 calsequestrin 2 (cardiac muscle)
CYB561 cytochrome b561
CYFIP2 cytoplasmic FMR1 interacting protein 2
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
HNF4A hepatocyte nuclear factor 4, alpha
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
IFT20 intraflagellar transport 20
KCNJ12 potassium channel, inwardly rectifying subfamily J, member 12
KEL Kell blood group, metallo-endopeptidase
LIX1L Lix1 homolog (chicken) like
LOC102723475 putative uncharacterized protein LOC388820
PHEX phosphate regulating endopeptidase homolog, X-linked
PHTF2 putative homeodomain transcription factor 2
RHCG Rh family, C glycoprotein
SCNN1B sodium channel, non voltage gated 1 beta subunit
SLC26A3 solute carrier family 26 (anion exchanger), member 3
STK39 serine threonine kinase 39
TGFB1 transforming growth factor, beta 1
USH1C Usher syndrome 1C (autosomal recessive, severe)
WNK4 WNK lysine deficient protein kinase 4