General Paralysis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0205858
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Genes

12 genes associated with the disease General Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
ATN1 atrophin 1
CD86 CD86 molecule
CXCL13 chemokine (C-X-C motif) ligand 13
DYSF dysferlin
FUS FUS RNA binding protein
IRF3 interferon regulatory factor 3
IRF7 interferon regulatory factor 7
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SOD1 superoxide dismutase 1, soluble
TARDBP TAR DNA binding protein
TNF tumor necrosis factor