Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
0.300 Biomarker disease CTD_human Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. 28604731 2017
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A
0.300 Biomarker disease CTD_human Genetics of caffeine consumption and responses to caffeine. 20532872 2010
Entrez Id: 4010
Gene Symbol: LMX1B
LMX1B
0.300 Biomarker disease CTD_human Nail-patella syndrome with an emphasis on the risk of renal and ocular findings. 20199424 2010
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3
0.300 Biomarker disease CTD_human Functional characterization of the new human GABA(A) receptor mutation beta3(R192H). 12189488 2002
Entrez Id: 3060
Gene Symbol: HCRT
HCRT
0.030 Biomarker disease BEFREE Research on the development of orexin receptor antagonists has dramatically increased with the approval of suvorexant for the treatment of primary insomnia. 31782044 2019
Entrez Id: 3060
Gene Symbol: HCRT
HCRT
0.030 Biomarker disease BEFREE The orally active dual OX<sub>1</sub>R and OX<sub>2</sub>R antagonist, almorexant, targets the orexin system for the treatment of primary insomnia. 28735928 2017
Entrez Id: 3060
Gene Symbol: HCRT
HCRT
0.030 Biomarker disease BEFREE A mechanistic hypothesis coupled with an in vitro assay to assess bioactivation led to replacement of the fluoroquinazoline ring of 10 with a chlorobenzoxazole to provide 3 (MK-4305), a potent dual orexin receptor antagonist that is currently being tested in phase III clinical trials for the treatment of primary insomnia. 20565075 2010
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
0.010 GeneticVariation disease BEFREE To investigate the relationship between exonic variant (rs4290270) in the tryptophan hydroxylase-2 gene and primary insomnia and symptoms of depression in Han Chinese. 29952309 2018
Entrez Id: 5715
Gene Symbol: PSMD9
PSMD9
0.010 GeneticVariation disease BEFREE We aimed at determining PSMD9 rs74421874/rs3825172/rs14259 SNPs potential linkage to primary insomnia and sleep hours in T2D families. 26166263 2015