increased urine osmolality Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the amount of ions in the urine compared to the normal state (Mammalian Phenotype Ontology, MP_0008055)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008055
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Genes

8 gene mutations causing the increased urine osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR1 angiotensin II receptor, type 1
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
FERMT1 fermitin family member 1
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
MMP17 matrix metallopeptidase 17 (membrane-inserted)
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC26A7 solute carrier family 26 (anion exchanger), member 7
TMEM27 transmembrane protein 27