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
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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