decreased urine potassium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal amount of potassium in the urine (Mammalian Phenotype Ontology, MP_0005618)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005618
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Genes

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

Symbol Name
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)
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
UPK2 uroplakin 2
VAV3 vav 3 guanine nucleotide exchange factor
WNK4 WNK lysine deficient protein kinase 4