hypermagnesemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally increased magnesium concentration in the blood. (Human Phenotype Ontology, HP_0002918)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002918
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Genes

3 genes associated with the hypermagnesemia 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
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)