Hypomagnesemia Gene Set
Genes
16 genes associated with the disease Hypomagnesemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTN4
|
actinin, alpha 4
|
|
ATP1A1
|
ATPase, Na+/K+ transporting, alpha 1 polypeptide
|
|
CLDN16
|
claudin 16
|
|
CLDN19
|
claudin 19
|
|
CNNM2
|
cyclin and CBS domain divalent metal cation transport mediator 2
|
|
EGF
|
epidermal growth factor
|
|
FIGF
|
c-fos induced growth factor (vascular endothelial growth factor D)
|
|
FXYD2
|
FXYD domain containing ion transport regulator 2
|
|
FXYD6-FXYD2
|
FXYD6-FXYD2 readthrough
|
|
HNF1B
|
HNF1 homeobox B
|
|
IFT122
|
intraflagellar transport 122
|
|
PCBD1
|
pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
|
|
PKD2
|
polycystic kidney disease 2 (autosomal dominant)
|
|
SLC12A3
|
solute carrier family 12 (sodium/chloride transporter), member 3
|
|
TRPM6
|
transient receptor potential cation channel, subfamily M, member 6
|
|
TRPM7
|
transient receptor potential cation channel, subfamily M, member 7
|
