Neuroligin-1 is a protein that in humans is encoded by the NLGN1 gene.[5][6][7]
This gene encodes a member of the neuroligin family of neuronal cell surface proteins. Neuroligin-1 acts as splice site-specific ligand for β-neurexins and has been shown to localize to the postsynaptic compartment at excitatory synapses and is involved in the formation and remodeling of central nervous system synapses.[7][8]
^ abcGRCh38: Ensembl release 89: ENSG00000169760 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000063887 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Philibert RA, Winfield SL, Sandhu HK, Martin BM, Ginns EI (April 2000). "The structure and expression of the human neuroligin-3 gene". Gene. 246 (1–2): 303–10. doi:10.1016/S0378-1119(00)00049-4. PMID 10767552.
^Nagase T, Kikuno R, Ishikawa K, Hirosawa M, Ohara O (April 2000). "Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 7 (2): 143–50. doi:10.1093/dnares/7.2.143. PMID 10819331.
^ ab"Entrez Gene: NLGN1 neuroligin 1".
^Scheiffele P, Fan J, Choih J, Fetter R, Serafini T (June 2000). "Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons". Cell. 101 (6): 657–69. doi:10.1016/S0092-8674(00)80877-6. PMID 10892652. S2CID 16095623.
Neuroligin-1 is a protein that in humans is encoded by the NLGN1 gene. This gene encodes a member of the neuroligin family of neuronal cell surface proteins...
gene for neuroligin. The known neuroligin genes in Homo sapiens include NLGN1, NLGN2, NLGN3, NLGN4X and NLGN5 (also known as NLGN4Y). Each gene has been...
(e.g., NLGN1, for neuroligin1). Protein designations are the same as the gene symbol, but are not italicised; all letters are in uppercase (NLGN1). mRNAs...
(NRXN1 mutations and brain disorders). NRXN1 has been shown to interact with NLGN1. GRCh38: Ensembl release 89: ENSG00000179915 – Ensembl, May 2017 GRCm38:...
components of synaptic transmission. For example, the first neuroligin (NLGN1) discovered was identified by its PDZ domain which binds to PSD95, a well-known...
relating to ASD in mice exposed to valproate in utero are NRXN1, NRXN2, NRXN3, NLGN1, NLGN2, and NLGN3. In the somatosensory cortex, CA1, dentate gyrus, and...
decrease neuronal density. Malat1 acts by regulating the expression levels of Nlgn1 and SynCAM1 which are important genes in synapse formation. Bromodomain...