fatal familial insomnia 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_0050433)
Similar Terms
Downloads & Tools

Genes

27 genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PRNP prion protein 2.9077
PNMA2 paraneoplastic Ma antigen 2 1.09083
MARK4 MAP/microtubule affinity-regulating kinase 4 0.97212
GDI1 GDP dissociation inhibitor 1 0.847078
HCRT hypocretin (orexin) neuropeptide precursor 0.846669
MSMB microseminoprotein, beta- 0.819616
PRND prion protein 2 (dublet) 0.760639
YWHAB tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta 0.700722
CPEB1 cytoplasmic polyadenylation element binding protein 1 0.671925
TPH1 tryptophan hydroxylase 1 0.623751
TXNDC9 thioredoxin domain containing 9 0.610057
PVALB parvalbumin 0.517649
PER2 period circadian clock 2 0.509192
PRODH proline dehydrogenase (oxidase) 1 0.501909
NMT1 N-myristoyltransferase 1 0.446935
NDP Norrie disease (pseudoglioma) 0.433772
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 0.383708
HSF4 heat shock transcription factor 4 0.35082
ENO2 enolase 2 (gamma, neuronal) 0.321909
PER3 period circadian clock 3 0.311014
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.273664
ADAM10 ADAM metallopeptidase domain 10 0.265494
MCM8 minichromosome maintenance complex component 8 0.261952
AIF1 allograft inflammatory factor 1 0.25207
GH1 growth hormone 1 0.245396
MAP4 microtubule-associated protein 4 0.185313
ERAS ES cell expressed Ras 0.181222