hypomagnesemia Gene Set
Genes
12 genes associated with the hypomagnesemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CASR
|
calcium-sensing receptor
|
|
CLDN16
|
claudin 16
|
|
CLDN19
|
claudin 19
|
|
EGF
|
epidermal growth factor
|
|
FXYD2
|
FXYD domain containing ion transport regulator 2
|
|
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
|
