NLGN3, neuroligin 3, 54413

N. diseases: 63; N. variants: 7
Disease: Pervasive Development Disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.050 GeneticVariation group BEFREE Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment. 31184401 2019
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.050 GeneticVariation group BEFREE Sleep/Wake Physiology and Quantitative Electroencephalogram Analysis of the Neuroligin-3 Knockout Rat Model of Autism Spectrum Disorder. 28958035 2017
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.050 Biomarker group BEFREE High resolution magnetic resonance imaging for characterization of the neuroligin-3 knock-in mouse model associated with autism spectrum disorder. 25299583 2014
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.050 GeneticVariation group BEFREE We conclude that there is no evidence for an involvement of NLGN3 and NLGN4X genetic variants with autism spectrum disorder on high functioning level in our study group. 18189281 2008
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder 		0.050 GeneticVariation group BEFREE A recent study reported that a mutation of neuroligin-3 (NL3), an X-linked gene, was found in siblings with autistic spectrum disorder in which two affected brothers had a point mutation that substituted a Cys for Arg451. 15152050 2004