abnormal urine creatinine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of creatinine in the urine (Mammalian Phenotype Ontology, MP_0011469)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011469
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Genes

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

Symbol Name
ADCY6 adenylate cyclase 6
AGTR1 angiotensin II receptor, type 1
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
BCAT2 branched chain amino-acid transaminase 2, mitochondrial
CLCN5 chloride channel, voltage-sensitive 5
CYBB cytochrome b-245, beta polypeptide
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase)
HRAS Harvey rat sarcoma viral oncogene homolog
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
NFE2L2 nuclear factor, erythroid 2-like 2
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme
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)
SLC16A10 solute carrier family 16 (aromatic amino acid transporter), member 10
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
UMOD uromodulin
UPK2 uroplakin 2