abnormal urine magnesium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of magnesium in the urine (Mammalian Phenotype Ontology, MP_0011434)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011434
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Genes

8 gene mutations causing the abnormal urine magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MTSS1 metastasis suppressor 1
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
STK39 serine threonine kinase 39
TRPM7 transient receptor potential cation channel, subfamily M, member 7
UMOD uromodulin