abnormal urine urea nitrogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of nitrogen in the form of urea in the urine (Mammalian Phenotype Ontology, MP_0011465)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011465
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Genes

11 gene mutations causing the abnormal urine urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY6 adenylate cyclase 6
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
JAK1 Janus kinase 1
SCTR secretin receptor
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
SLC14A2 solute carrier family 14 (urea transporter), member 2
SLC25A23 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
TMEM27 transmembrane protein 27
UMOD uromodulin