orthostatic hypotension Gene Set
Genes
12 genes associated with the orthostatic hypotension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AAAS
|
achalasia, adrenocortical insufficiency, alacrimia
|
|
ATP7A
|
ATPase, Cu++ transporting, alpha polypeptide
|
|
CAV1
|
caveolin 1, caveolae protein, 22kDa
|
|
CYP11B2
|
cytochrome P450, family 11, subfamily B, polypeptide 2
|
|
DBH
|
dopamine beta-hydroxylase (dopamine beta-monooxygenase)
|
|
GMPPA
|
GDP-mannose pyrophosphorylase A
|
|
HEXB
|
hexosaminidase B (beta polypeptide)
|
|
IKBKAP
|
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
|
|
LMNB1
|
lamin B1
|
|
NTRK1
|
neurotrophic tyrosine kinase, receptor, type 1
|
|
SNCA
|
synuclein, alpha (non A4 component of amyloid precursor)
|
|
TTR
|
transthyretin
|
