Gene: NLGN3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3 		0.100 CausalMutation phenotype CLINVAR Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients. 24570023 2014
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3 		0.100 CausalMutation phenotype CLINVAR Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. 23849776 2013
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3 		0.100 CausalMutation phenotype CLINVAR Disorder-associated mutations lead to functional inactivation of neuroligins. 15150161 2004
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3 		0.100 CausalMutation phenotype CLINVAR Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. 12669065 2003