abnormal magnesium ion homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the processes involved in the maintenance of an internal equilibrium of magnesium ions within the body or between a cell and its external environment (Mammalian Phenotype Ontology, MP_0011979)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011979
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22 gene mutations causing the abnormal magnesium ion homeostasis 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