abnormal urine potassium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of potassium in the urine (Mammalian Phenotype Ontology, MP_0004820)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004820
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Genes

27 gene mutations causing the abnormal urine potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
ADCY6 adenylate cyclase 6
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide
CLDN7 claudin 7
CLN3 ceroid-lipofuscinosis, neuronal 3
CYP4A11 cytochrome P450, family 4, subfamily A, polypeptide 11
GUCA2B guanylate cyclase activator 2B (uroguanylin)
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SCTR secretin receptor
SGK1 serum/glucocorticoid regulated kinase 1
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
STK39 serine threonine kinase 39
TFCP2L1 transcription factor CP2-like 1
TGFB1 transforming growth factor, beta 1
UMOD uromodulin
UPK2 uroplakin 2
VAV3 vav 3 guanine nucleotide exchange factor
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
WNK4 WNK lysine deficient protein kinase 4