Metabolic Alkalosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0220983
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Genes

26 genes associated with the disease Metabolic Alkalosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALB albumin
BSND barttin CLCNK-type chloride channel accessory beta subunit
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CLCN2 chloride channel, voltage-sensitive 2
CLCNKB chloride channel, voltage-sensitive Kb
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
GAST gastrin
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
INSR insulin receptor
INSRR insulin receptor-related receptor
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
NARS2 asparaginyl-tRNA synthetase 2, mitochondrial (putative)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
POMC proopiomelanocortin
REN renin
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4