Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10522
Gene Symbol: DEAF1
DEAF1
0.100 GeneticVariation phenotype CLINVAR Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype. 28940898 2017
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 79158
Gene Symbol: GNPTAB
GNPTAB
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 79813
Gene Symbol: EHMT1
EHMT1
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 64207
Gene Symbol: IRF2BPL
IRF2BPL
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 825
Gene Symbol: CAPN3
CAPN3
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 2643
Gene Symbol: GCH1
GCH1
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 2892
Gene Symbol: GRIA3
GRIA3
0.100 GeneticVariation phenotype CLINVAR A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability. 29016847 2017
Entrez Id: 348
Gene Symbol: APOE
APOE
0.060 GeneticVariation phenotype BEFREE Genetic association between APOE-ϵ4 genotype and sleep disturbances was assessed using unadjusted linear regression models. 26314507 2015
Entrez Id: 9575
Gene Symbol: CLOCK
CLOCK
0.060 GeneticVariation phenotype BEFREE Sleep disturbances in major depressive disorder (MDD) are characterized by increased sleep latency, poorer sleep efficiency reduced latency to the first rapid eye movement (REM) sleep episode, and early-morning awakening, but there is little data to indicate a role of circadian clock genes in MDD. 17969870 2007
Entrez Id: 348
Gene Symbol: APOE
APOE
0.060 GeneticVariation phenotype BEFREE This investigation found a significant relationship between presence of APOE ε4 allele and objective sleep disturbances measured by both actigraphy and PSG, but not subjective sleep complaints in a healthy population screened for dementia. 27777343 2016
Entrez Id: 9575
Gene Symbol: CLOCK
CLOCK
0.060 GeneticVariation phenotype BEFREE The main positive findings refer to associations between selected polymorphisms and: 1) chronotype with the ARNTL gene (rs11824092 and rs1481892) and the CLOCK (rs1268271) 2) sleep duration with the CLOCK gene (rs3805148) and the TIM gene (rs2291739) 3) daytime dysfunction with the PER3 gene (rs228727, rs228642, rs10864315) 4) subjective sleep quality with the ARNTL gene (rs11824092, rs1982350) 5) sleep disturbances with the ARNTL gene (rs11600996) We also found the significant epistatic interactions between polymorphism of the PER3 gene (rs2640909) & the CLOCK gene (rs11932595) and following sleep quality variables: sleep duration, habitual sleep efficiency and subjective sleep quality. 27102916 2016
Entrez Id: 9575
Gene Symbol: CLOCK
CLOCK
0.060 GeneticVariation phenotype BEFREE 3111T/C clock gene polymorphism is not associated with sleep disturbances in untreated depressed patients. 20370469 2010
Entrez Id: 9575
Gene Symbol: CLOCK
CLOCK
0.060 GeneticVariation phenotype BEFREE Physiology and behaviour are critically dependent on circadian regulation via a core set of clock genes, dysregulation of which leads to metabolic and sleep disturbances. 29982483 2018
Entrez Id: 348
Gene Symbol: APOE
APOE
0.060 GeneticVariation phenotype BEFREE To determine whether sleep medication mediates the risk of developing MCI for individuals with sleep disturbance and/or APOE <sub>e4</sub>, we analyzed the National Alzheimer's Coordinating Center Uniform Data Set. 30359892 2018
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.050 GeneticVariation phenotype BEFREE Linear regression was used to assess the effect of the IL-6 genotype and other covariates on mean fatigue and sleep disturbance scores. 20570482 2010
Entrez Id: 8863
Gene Symbol: PER3
PER3
0.040 GeneticVariation phenotype BEFREE One balanced translocation carrier parent had disruption of the period homolog 3 (PER3) gene and reported sleep disturbances. 18958851 2008
Entrez Id: 8863
Gene Symbol: PER3
PER3
0.040 GeneticVariation phenotype BEFREE The main positive findings refer to associations between selected polymorphisms and: 1) chronotype with the ARNTL gene (rs11824092 and rs1481892) and the CLOCK (rs1268271) 2) sleep duration with the CLOCK gene (rs3805148) and the TIM gene (rs2291739) 3) daytime dysfunction with the PER3 gene (rs228727, rs228642, rs10864315) 4) subjective sleep quality with the ARNTL gene (rs11824092, rs1982350) 5) sleep disturbances with the ARNTL gene (rs11600996) We also found the significant epistatic interactions between polymorphism of the PER3 gene (rs2640909) & the CLOCK gene (rs11932595) and following sleep quality variables: sleep duration, habitual sleep efficiency and subjective sleep quality. 27102916 2016
Entrez Id: 8863
Gene Symbol: PER3
PER3
0.040 GeneticVariation phenotype BEFREE Furthermore, analyzing patients with sleep disturbance at the baseline (PSQI >5) revealed that only the PER3(5) noncarriers exhibited a significant improvement in overall PSQI scores. 26440425 2015
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.030 GeneticVariation phenotype BEFREE The role of serotonin transporter and its functional gene polymorphism (5-HTTLPR, serotonin transporter linked polymorphic region) was investigated in sleep disturbances in various mental disorders, with conflicting findings. 30948693 2019
Entrez Id: 6532
Gene Symbol: SLC6A4
SLC6A4
0.030 GeneticVariation phenotype BEFREE Direct associations were identified between the dopamine receptor 3 (DRD3) BalI polymorphism and depression; the dopamine receptor 1 (DRD1) and dopamine transporter gene 3' VNTR polymorphisms and aberrant motor behavior; the DRD4 VNTR and sleep disturbances; and the SERT gene VNTR 5HTTLPR and apathy items. 20685009 2012
Entrez Id: 8914
Gene Symbol: TIMELESS
TIMELESS
0.030 GeneticVariation phenotype BEFREE The main positive findings refer to associations between selected polymorphisms and: 1) chronotype with the ARNTL gene (rs11824092 and rs1481892) and the CLOCK (rs1268271) 2) sleep duration with the CLOCK gene (rs3805148) and the TIM gene (rs2291739) 3) daytime dysfunction with the PER3 gene (rs228727, rs228642, rs10864315) 4) subjective sleep quality with the ARNTL gene (rs11824092, rs1982350) 5) sleep disturbances with the ARNTL gene (rs11600996) We also found the significant epistatic interactions between polymorphism of the PER3 gene (rs2640909) & the CLOCK gene (rs11932595) and following sleep quality variables: sleep duration, habitual sleep efficiency and subjective sleep quality. 27102916 2016
Entrez Id: 57107
Gene Symbol: PDSS2
PDSS2
0.030 GeneticVariation phenotype BEFREE In addition to the genotypes of rs671, the patients were assessed with the PD sleep scale-2nd version (PDSS-2) and the Epworth sleepiness scale (ESS) for symptoms of daytime and nocturnal sleep disturbances. 31831791 2019
Entrez Id: 8914
Gene Symbol: TIMELESS
TIMELESS
0.030 GeneticVariation phenotype BEFREE Six missense changes were detected only in individuals with ASD with sleep disturbance: p.F498S in TIMELESS, p.S20R in NR1D1, p.R493C in PER3, p.H542R in CLOCK, p.L473S in ARNTL2, and p.A325V in MTNR1B. 25957987 2016