akinetic mutism Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness. (Human Disease Ontology, DOID_4267)
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Genes

17 genes co-occuring with the disease akinetic mutism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRNP prion protein 1.85638
TXNDC9 thioredoxin domain containing 9 1.52424
PNMA2 paraneoplastic Ma antigen 2 1.37338
MYBPC1 myosin binding protein C, slow type 1.31144
ACAA2 acetyl-CoA acyltransferase 2 1.20396
ENO2 enolase 2 (gamma, neuronal) 1.19186
RGMB repulsive guidance molecule family member b 0.931656
MRS2 MRS2 magnesium transporter 0.906086
MAPT microtubule-associated protein tau 0.617877
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.426265
TARDBP TAR DNA binding protein 0.393374
ARSA arylsulfatase A 0.37629
APOE apolipoprotein E 0.363716
CBS cystathionine-beta-synthase 0.291898
GBA glucosidase, beta, acid 0.235268
CP ceruloplasmin (ferroxidase) 0.165001
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 0.160021