abnormal circulating magnesium level Gene Set
Genes
22 gene mutations causing the abnormal circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ACTR6
|
ARP6 actin-related protein 6 homolog (yeast)
|
|
AKR1B1
|
aldo-keto reductase family 1, member B1 (aldose reductase)
|
|
BBS4
|
Bardet-Biedl syndrome 4
|
|
CALCB
|
calcitonin-related polypeptide beta
|
|
CASR
|
calcium-sensing receptor
|
|
CLDN16
|
claudin 16
|
|
GIT2
|
G protein-coupled receptor kinase interacting ArfGAP 2
|
|
KEL
|
Kell blood group, metallo-endopeptidase
|
|
LONRF3
|
LON peptidase N-terminal domain and ring finger 3
|
|
MTA3
|
metastasis associated 1 family, member 3
|
|
SCG5
|
secretogranin V
|
|
SLC12A1
|
solute carrier family 12 (sodium/potassium/chloride transporter), member 1
|
|
SLC12A3
|
solute carrier family 12 (sodium/chloride transporter), member 3
|
|
SLC20A2
|
solute carrier family 20 (phosphate transporter), member 2
|
|
SLC2A9
|
solute carrier family 2 (facilitated glucose transporter), member 9
|
|
STK39
|
serine threonine kinase 39
|
|
TRIM45
|
tripartite motif containing 45
|
|
TRMT10A
|
tRNA methyltransferase 10 homolog A (S. cerevisiae)
|
|
TRPM6
|
transient receptor potential cation channel, subfamily M, member 6
|
|
TRPM7
|
transient receptor potential cation channel, subfamily M, member 7
|
|
WNK4
|
WNK lysine deficient protein kinase 4
|
|
XK
|
X-linked Kx blood group
|
