abnormality of magnesium homeostasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of magnesium ion homeostasis. (Human Phenotype Ontology, HP_0004921)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004921
Similar Terms
Downloads & Tools

Genes

14 genes associated with the abnormality of magnesium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AP2S1 adaptor-related protein complex 2, sigma 1 subunit
CASR calcium-sensing receptor
CLDN16 claudin 16
CLDN19 claudin 19
EGF epidermal growth factor
FXYD2 FXYD domain containing ion transport regulator 2
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SARS2 seryl-tRNA synthetase 2, mitochondrial
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
TBCE tubulin folding cofactor E
TRPM6 transient receptor potential cation channel, subfamily M, member 6