Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
0.600 SusceptibilityMutation disease CLINVAR
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
0.600 Biomarker disease CTD_human
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 Biomarker group BEFREE TWIK-related spinal cord potassium channel is involved in migraine by screening the KCNK18 gene in subjects diagnosed with migraine. 23919895 2013
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 GeneticVariation group BEFREE KCNK18 (TRESK) genetic variants in Italian patients with migraine. 25324165 2014
CUI: C2349453
Disease: Familial migraine
Familial migraine
0.020 GeneticVariation disease BEFREE A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. 20871611 2010
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
0.600 GeneticVariation disease CLINVAR A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura. 20871611 2010
CUI: C0278134
Disease: Absence of sensation
Absence of sensation
0.010 Biomarker phenotype BEFREE A role has been suggested for the two-pore domain (K2P) potassium channel, TWIK-related spinal cord potassium channel (TRESK, encoded by KCNK18), in pain pathways and general anaesthesia. 20871611 2010
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 GeneticVariation group BEFREE A single migraine study using a candidate-gene approach was performed in 2010 identifying a rare mutation in the TRESK potassium channel segregating in a large family with migraine with aura, but this finding has later become questioned. 28255817 2017
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
0.050 GeneticVariation disease BEFREE A single migraine study using a candidate-gene approach was performed in 2010 identifying a rare mutation in the TRESK potassium channel segregating in a large family with migraine with aura, but this finding has later become questioned. 28255817 2017
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE Additional evidence of a biological role of TRESK channels was provided by behavioral evidence of pain (flinching and licking), in vivo electrophysiological evidence of C-nociceptor activation following IBA injection in the rat hindpaw, and increased sensitivity to painful pressure after TRESK knockdown in vivo. 21527011 2011
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 Biomarker disease BEFREE Changes in the expression of the potassium channels TASK1, TASK3 and TRESK in a rat model of oral squamous cell carcinoma and their relation to malignancy. 30818127 2019
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 Biomarker group BEFREE Collectively, our findings provide evidence for a role of TRESK in migraine pathogenesis and its suitability as a therapeutic target. 31742594 2019
CUI: C0020429
Disease: Hyperalgesia
Hyperalgesia
0.010 AlteredExpression phenotype BEFREE Compared with SNI rats, intrathecal injection of TRESK gene recombinant adenovirus significantly downregulated the expression levels of Cx36 and Cx43 and suppressed the activation of gliocytes in the spinal cord, with hyperalgesia significantly reduced. 28160200 2017
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
0.600 Biomarker disease GENOMICS_ENGLAND Functional analysis of missense variants in the TRESK (KCNK18) K channel. 22355750 2012
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13
0.600 Biomarker disease GENOMICS_ENGLAND Functional analysis of missense variants in the TRESK (KCNK18) K channel. 22355750 2012
CUI: C0596240
Disease: Cancer Pain
Cancer Pain
0.010 Biomarker phenotype BEFREE Here, we found that the reduced abundance of potassium channels called TRESK in dorsal root ganglion (DRG) neurons sensitized nociceptive sensory neurons and cancer-associated pain. 30327410 2018
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 Biomarker group BEFREE Here, we identify a new mechanism, termed frameshift mutation-induced alternative translation initiation (fsATI), that may explain why only TRESK-MT is associated with migraine. fsATI leads to the production of a second protein fragment, TRESK-MT2, which co-assembles with and inhibits TREK1 and TREK2, two other two-pore-domain K+ channels, to increase trigeminal sensory neuron excitability, leading to a migraine-like phenotype in rodents. 30573346 2019
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 AlteredExpression group BEFREE In situ hybridization studies of the mouse Kcnk18 ortholog show that it is developmentally expressed in the trigeminal and dorsal root ganglia, further supporting the involvement of this gene in migraine pathogenesis. 23030542 2012
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 GeneticVariation group BEFREE In this issue of Neuron, Royal et al.(2018) find that a mutant form of the TRESK ion channel linked to migraine undergoes alternative translation to produce an inhibitory protein that blocks TREK channels, leading to neuronal hyperexcitability and migraine in rodents. 30653930 2019
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.100 GeneticVariation group BEFREE In this study, three common polymorphisms in the KCNK18 gene were analysed for genetic variation in an Australian case-control migraine population consisting of 340 migraine cases and 345 controls. 23911303 2013
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE Intrathecal application of exogenous calcineurin to tumor-bearing rats rescued TRESK abundance and abrogated both DRG hyperexcitability and pain hypersensitivity, whereas either inhibition or knockdown of calcineurin in normal rats reduced TRESK abundance and increased DRG excitability and pain sensitivity. 30327410 2018
Hemiplegic migraine, familial type 1
0.010 GeneticVariation disease BEFREE On the other hand, the presence of KCNK18 mutation indicated another FHM subtype. 26747084 2016
CUI: C2349453
Disease: Familial migraine
Familial migraine
0.020 GeneticVariation disease BEFREE Other genes displayed enriched expression in the trigeminal compared to dorsal root ganglion, and in-depth transcriptomic analysis of the KCNK18 gene underlying familial migraine shows selective neural expression within two specific populations of ganglionic neurons. 28699403 2018
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura
0.050 GeneticVariation disease BEFREE Our study shows the presence of several KCNK18 gene mutations in both migraine with aura and migraine without aura. 25324165 2014
CUI: C0338480
Disease: Common Migraine
Common Migraine
0.020 GeneticVariation disease BEFREE Our study shows the presence of several KCNK18 gene mutations in both migraine with aura and migraine without aura. 25324165 2014