Hypermagnesemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormally increased magnesium concentration in the blood. (Human Phenotype Ontology, HP_0002918)
External Link https://www.disgenet.org/browser/0/1/0/C1522135
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Genes

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

Symbol Name
ALB albumin
ALDOB aldolase B, fructose-bisphosphate
AP2S1 adaptor-related protein complex 2, sigma 1 subunit
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1
CASR calcium-sensing receptor
CLCNKB chloride channel, voltage-sensitive Kb
CLDN10 claudin 10
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
LPA lipoprotein, Lp(a)
PTH parathyroid hormone
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC30A10 solute carrier family 30, member 10
SLC39A14 solute carrier family 39 (zinc transporter), member 14