Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112755
Gene Symbol: STX1B
STX1B
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies. 27781031

2016
Entrez Id: 112755
Gene Symbol: STX1B
STX1B
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. 25362483

2014
Entrez Id: 112755
Gene Symbol: STX1B
STX1B
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Characterization of a presynaptic glutamate receptor. 8105537

1993