Supranuclear Palsy, Progressive Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

28 genes associated with the Supranuclear Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACP2 acid phosphatase 2, lysosomal
APOE apolipoprotein E
ATXN2 ataxin 2
C9ORF72 chromosome 9 open reading frame 72
CRHR1 corticotropin releasing hormone receptor 1
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DDB2 damage-specific DNA binding protein 2, 48kDa
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GBA glucosidase, beta, acid
GRN granulin
LRRK2 leucine-rich repeat kinase 2
MAPT microtubule-associated protein tau
MOBP myelin-associated oligodendrocyte basic protein
NAT1 N-acetyltransferase 1 (arylamine N-acetyltransferase)
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2
NSF N-ethylmaleimide-sensitive factor
PARK2 parkin RBR E3 ubiquitin protein ligase
PINK1 PTEN induced putative kinase 1
PON1 paraoxonase 1
PON2 paraoxonase 2
SOD1 superoxide dismutase 1, soluble
SOD2 superoxide dismutase 2, mitochondrial
SPPL2C signal peptide peptidase like 2C
STX6 syntaxin 6
VEGFA vascular endothelial growth factor A
WNT3 wingless-type MMTV integration site family, member 3