Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
0.120 Biomarker disease BEFREE Frameshift and missense mutations in the X-linked neuroligin 4 (NLGN4, MIM# 300427) and neuroligin 3 (NLGN3, MIM# 300336) genes have been identified in patients with autism, Asperger syndrome and mental retardation. 18628683 2008
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
0.120 GeneticVariation disease BEFREE The phenotypes of genes causing syndromic and non-syndromic mental retardation (NLGN3, NLGN4, RPS6KA3(RSK2), OPHN1, ATRX, SLC6A8, ARX, SYN1, AGTR2, MECP2, PQBP1, SMCX, and SLC16A2) are first discussed, as these may be the focus of more targeted mutation analysis. 16118346 2006
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
0.120 GeneticVariation disease CLINVAR