STX1B, syntaxin 1B, 112755

N. diseases: 58; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures
0.140 Biomarker phenotype BEFREE A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B. 30009426 2018
CUI: C0036572
Disease: Seizures
Seizures
0.140 Biomarker phenotype BEFREE These findings further demonstrate that STX1B protein levels are negatively correlated with a seizure and can decrease the sensitivity of the photosensitive response in a PTZ-induced seizure zebrafish larvae; furthermore, STX1B may partially mediate the anticonvulsant effect of BBR. 30534049 2018
CUI: C0036572
Disease: Seizures
Seizures
0.140 GeneticVariation phenotype BEFREE TMS measures of motor cortical excitability show utility in demonstrating normal excitability in adult STX1B mutation carriers with history of seizures. 29101845 2017
CUI: C0036572
Disease: Seizures
Seizures
0.140 Biomarker phenotype BEFREE Video and local field potential analyses of zebrafish larvae with antisense knockdown of stx1b showed seizure-like behavior and epileptiform discharges that were highly sensitive to increased temperature. 25362483 2014
CUI: C0036572
Disease: Seizures
Seizures
0.140 GeneticVariation phenotype CLINVAR
CUI: C0036572
Disease: Seizures
Seizures
0.140 CausalMutation phenotype CLINVAR