decreased circulating renin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An decreased level of renin (PRO:000013883) in the blood. (Human Phenotype Ontology, HP_0003351)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003353
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Genes

8 gene mutations causing the decreased circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR1 angiotensin II receptor, type 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
NPR1 natriuretic peptide receptor 1
REN renin
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC4A5 solute carrier family 4 (sodium bicarbonate cotransporter), member 5
SUCNR1 succinate receptor 1
TGFB1 transforming growth factor, beta 1