brain stem infarction Gene Set

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

26 genes co-occuring with the disease brain stem infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FGB fibrinogen beta chain 0.88434
OR10R2 olfactory receptor, family 10, subfamily R, member 2 0.825768
CRLF1 cytokine receptor-like factor 1 0.78066
CLEC3A C-type lectin domain family 3, member A 0.760639
CLEC2B C-type lectin domain family 2, member B 0.754934
CLEC10A C-type lectin domain family 10, member A 0.729762
CANX calnexin 0.720865
PNMA2 paraneoplastic Ma antigen 2 0.692296
PLAT plasminogen activator, tissue 0.658026
CDSN corneodesmosin 0.65288
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 0.537731
GLA galactosidase, alpha 0.49274
MEFV Mediterranean fever 0.403811
POMC proopiomelanocortin 0.402318
CD22 CD22 molecule 0.400826
APOH apolipoprotein H (beta-2-glycoprotein I) 0.365932
F3 coagulation factor III (thromboplastin, tissue factor) 0.352291
LEP leptin 0.318272
MMP3 matrix metallopeptidase 3 0.241895
PRTN3 proteinase 3 0.23666
LPA lipoprotein, Lp(a) 0.222822
COG2 component of oligomeric golgi complex 2 0.210925
PROS1 protein S (alpha) 0.209918
TH tyrosine hydroxylase 0.192344
TAC1 tachykinin, precursor 1 0.18151
CD19 CD19 molecule 0.145517