central pontine myelinolysis Gene Set

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

19 genes co-occuring with the disease central pontine myelinolysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AVP arginine vasopressin 1.59787
FOXM1 forkhead box M1 1.48691
LIN37 lin-37 DREAM MuvB core complex component 1.39957
SLC8A2 solute carrier family 8 (sodium/calcium exchanger), member 2 1.16563
FLVCR2 feline leukemia virus subgroup C cellular receptor family, member 2 1.09587
AQP1 aquaporin 1 (Colton blood group) 0.983479
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 0.826589
MBP myelin basic protein 0.691094
SLC6A1 solute carrier family 6 (neurotransmitter transporter), member 1 0.679499
TRH thyrotropin-releasing hormone 0.66199
AQP4 aquaporin 4 0.618268
CABIN1 calcineurin binding protein 1 0.581996
MAG myelin associated glycoprotein 0.468063
CA2 carbonic anhydrase II 0.399334
FUT4 fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific) 0.286519
INS insulin 0.241196
B3GAT1 beta-1,3-glucuronyltransferase 1 0.207578
PTHLH parathyroid hormone-like hormone 0.198386
CP ceruloplasmin (ferroxidase) 0.185313