Hypochloremia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormally decreased chloride concentration in the blood. (Human Phenotype Ontology, HP_0003113)
External Link https://www.disgenet.org/browser/0/1/0/C0740895
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Genes

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

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
MAGED2 melanoma antigen family D2
SARS2 seryl-tRNA synthetase 2, mitochondrial
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC26A3 solute carrier family 26 (anion exchanger), member 3