hypotension Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Blood pressure that is abnormally low. (Experimental Factor Ontology, EFO_0005251)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001596
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Genes

23 gene mutations causing the hypotension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACE2 angiotensin I converting enzyme 2
ADRA1A adrenoceptor alpha 1A
ADRA1D adrenoceptor alpha 1D
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ARNTL aryl hydrocarbon receptor nuclear translocator-like
AVPR1A arginine vasopressin receptor 1A
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
DUSP1 dual specificity phosphatase 1
FGF2 fibroblast growth factor 2 (basic)
KLF3 Kruppel-like factor 3 (basic)
LEP leptin
NPAS2 neuronal PAS domain protein 2
NPR3 natriuretic peptide receptor 3
OXSR1 oxidative stress responsive 1
OXT oxytocin/neurophysin I prepropeptide
PPARA peroxisome proliferator-activated receptor alpha
PTGER2 prostaglandin E receptor 2 (subtype EP2), 53kDa
REN renin
RGS5 regulator of G-protein signaling 5
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
STK39 serine threonine kinase 39