NLGN3, neuroligin 3, 54413

N. diseases: 4; N. variants: 4
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0432072
Disease:
Dysmorphic features 		TG 0.700 CausalMutation CLINVAR Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients. 24570023 2014
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1849265
Disease:
Overgrowth 		TG 0.700 CausalMutation CLINVAR Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients. 24570023 2014
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1849265
Disease:
Overgrowth 		TG 0.700 CausalMutation CLINVAR Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. 23849776 2013
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0432072
Disease:
Dysmorphic features 		TG 0.700 CausalMutation CLINVAR Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. 23849776 2013
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1849265
Disease:
Overgrowth 		TG 0.700 CausalMutation CLINVAR Disorder-associated mutations lead to functional inactivation of neuroligins. 15150161 2004
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0432072
Disease:
Dysmorphic features 		TG 0.700 CausalMutation CLINVAR Disorder-associated mutations lead to functional inactivation of neuroligins. 15150161 2004
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1849265
Disease:
Overgrowth 		TG 0.700 CausalMutation CLINVAR Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. 12669065 2003
dbSNP: rs34927195
rs34927195
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0432072
Disease:
Dysmorphic features 		TG 0.700 CausalMutation CLINVAR Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. 12669065 2003
dbSNP: rs121917893
rs121917893
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1845540
Disease:
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 1 (finding) 		T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs121917893
rs121917893
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1845341
Disease:
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) 		T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1569485503
rs1569485503
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0856975
Disease:
Autistic behavior 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1569485503
rs1569485503
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C1843367
Disease:
Poor school performance 		T 0.700 CausalMutation CLINVAR
dbSNP: rs878853147
rs878853147
Entrez Id: 54413
Gene Symbol: NLGN3
NLGN3
CUI: C0025362
Disease:
Mental Retardation 		T 0.700 GeneticVariation CLINVAR