dysautonomia Gene Set
Genes
14 genes associated with the dysautonomia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AAAS
|
achalasia, adrenocortical insufficiency, alacrimia
|
|
ATXN3
|
ataxin 3
|
|
BRAT1
|
BRCA1-associated ATM activator 1
|
|
ECE1
|
endothelin converting enzyme 1
|
|
GLA
|
galactosidase, alpha
|
|
GMPPA
|
GDP-mannose pyrophosphorylase A
|
|
LIFR
|
leukemia inhibitory factor receptor alpha
|
|
LMNB1
|
lamin B1
|
|
NTRK1
|
neurotrophic tyrosine kinase, receptor, type 1
|
|
PRNP
|
prion protein
|
|
SCN11A
|
sodium channel, voltage gated, type XI alpha subunit
|
|
SNCA
|
synuclein, alpha (non A4 component of amyloid precursor)
|
|
TTR
|
transthyretin
|
|
WDR45
|
WD repeat domain 45
|
