Gene: STX1B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112755
Gene Symbol: STX1B
STX1B 		0.010 Biomarker disease 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