progressive bulbar palsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

25 genes co-occuring with the disease progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3 2.01568
SLC52A1 solute carrier family 52 (riboflavin transporter), member 1 1.71089
MUSK muscle, skeletal, receptor tyrosine kinase 1.34635
REEP1 receptor accessory protein 1 1.13501
CST7 cystatin F (leukocystatin) 0.986007
UBQLN2 ubiquilin 2 0.917199
HMBS hydroxymethylbilane synthase 0.854859
CPN1 carboxypeptidase N, polypeptide 1 0.650113
GPR162 G protein-coupled receptor 162 0.64577
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.619442
NPC2 Niemann-Pick disease, type C2 0.605372
CLEC3A C-type lectin domain family 3, member A 0.595623
CLEC2B C-type lectin domain family 2, member B 0.590169
SOD2 superoxide dismutase 2, mitochondrial 0.584719
TRH thyrotropin-releasing hormone 0.581217
CLEC10A C-type lectin domain family 10, member A 0.566054
NPC1 Niemann-Pick disease, type C1 0.471846
GSN gelsolin 0.408292
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1 0.360764
TARDBP TAR DNA binding protein 0.357446
ATXN3 ataxin 3 0.337608
ALB albumin 0.241895
GBA glucosidase, beta, acid 0.202618
CST3 cystatin C 0.175947
B3GAT1 beta-1,3-glucuronyltransferase 1 0.159658