Fabry Disease Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14499)
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Genes

13 genes associated with the Fabry Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
CRP C-reactive protein, pentraxin-related
GLA galactosidase, alpha
IL10 interleukin 10
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL6 interleukin 6
NOS3 nitric oxide synthase 3 (endothelial cell)
PON1 paraoxonase 1
TNF tumor necrosis factor
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor