Gene: STXBP5L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9515
Gene Symbol: STXBP5L
STXBP5L 		0.010 GeneticVariation group BEFREE Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder. 25504045 2015