amyotrophic neuralgia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_10383)
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Genes

29 genes co-occuring with the disease amyotrophic neuralgia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SEPT9 septin 9 2.64377
SEPT5 septin 5 1.87515
SEC14L1 SEC14-like 1 (S. cerevisiae) 1.77947
DNAH17 dynein, axonemal, heavy chain 17 1.66916
PMP22 peripheral myelin protein 22 1.62963
SEPT14 septin 14 1.31755
MPZ myelin protein zero 1.2717
SEPT11 septin 11 1.16478
RTKN rhotekin 1.15538
SRSF2 serine/arginine-rich splicing factor 2 1.08118
SEPT7 septin 7 1.06018
INA internexin neuronal intermediate filament protein, alpha 0.953273
SEPT1 septin 1 0.952021
PRX periaxin 0.926279
GALR2 galanin receptor 2 0.920498
AANAT aralkylamine N-acetyltransferase 0.872462
GJB1 gap junction protein, beta 1, 32kDa 0.813462
MTMR2 myotubularin related protein 2 0.764718
SRPX2 sushi-repeat containing protein, X-linked 2 0.756971
EGR2 early growth response 2 0.643404
TK1 thymidine kinase 1, soluble 0.608494
SULT2B1 sulfotransferase family, cytosolic, 2B, member 1 0.572273
NMU neuromedin U 0.565277
SPHK1 sphingosine kinase 1 0.516494
FOXL2 forkhead box L2 0.480945
VCL vinculin 0.41727
CYGB cytoglobin 0.347144
CAMP cathelicidin antimicrobial peptide 0.335778
TIMP2 TIMP metallopeptidase inhibitor 2 0.166768