decreased circulating mineralocorticoid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than normal blood concentration of corticosteroids that influence water and electrolyte metabolism and balance (Mammalian Phenotype Ontology, MP_0003374)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003374
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Genes

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

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
POMC proopiomelanocortin
SCNN1B sodium channel, non voltage gated 1 beta subunit
SLC4A5 solute carrier family 4 (sodium bicarbonate cotransporter), member 5
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
STAR steroidogenic acute regulatory protein
TGFB1 transforming growth factor, beta 1
WNK4 WNK lysine deficient protein kinase 4