increased circulating aldosterone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002666
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Genes

21 gene mutations causing the increased circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit
CLDN7 claudin 7
DKK3 dickkopf WNT signaling pathway inhibitor 3
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
KCNK3 potassium channel, two pore domain subfamily K, member 3
LOC102723475 putative uncharacterized protein LOC388820
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
NPR1 natriuretic peptide receptor 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NR3C2 nuclear receptor subfamily 3, group C, member 2
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
REN renin
SCNN1B sodium channel, non voltage gated 1 beta subunit
SGK1 serum/glucocorticoid regulated kinase 1
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
STK39 serine threonine kinase 39
TGFB1 transforming growth factor, beta 1
VAV2 vav 2 guanine nucleotide exchange factor
VAV3 vav 3 guanine nucleotide exchange factor