Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 GeneticVariation disease BEFREE Functional significance of rare neuroligin 1 variants found in autism. 28841651 2017
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 GeneticVariation disease BEFREE Correction: Functional significance of rare neuroligin 1 variants found in autism. 28972980 2017
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 Biomarker disease BEFREE NLGN1 has previously been associated with autism, and it encodes neuroligin 1, a protein involved in synaptogenesis, learning, and memory. 27219346 2016
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 GeneticVariation disease BEFREE Lastly, we identified differences in the dimerization capacity of autism-associated neuroligin mutants, and found that neuroligin 3 R471C mutants can form heterodimers with neuroligin 1. 22671294 2012
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 Biomarker disease CTD_human Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. 19404257 2009
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 Biomarker disease BEFREE Osmotic avoidance in Caenorhabditis elegans: synaptic function of two genes, orthologues of human NRXN1 and NLGN1, as candidates for autism. 20010541 2009
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 GeneticVariation disease LHGDN Here, we report a detailed molecular genetic analysis of NLGN1, NLGN3, NLGN4, and NLNG4Y in the Finnish autism sample. 16077734 2005
Entrez Id: 22871
Gene Symbol: NLGN1
NLGN1
0.360 GeneticVariation disease BEFREE The neuroligin gene family consists of five members (NLGN1 at 3q26, NLGN2 at 17p13, NLGN3 at Xq13, NLGN4 at Xp22, and NLGN4Y at Yq11), of which NLGN1 and NLGN3 are located within the best loci observed in our previous genome-wide scan for autism in the Finnish sample. 16077734 2005