NLGN2

NLGN2

A gene on chromosome 17p13.1 that encodes neuroligin 2, a neuronal cell surface protein involved in cell–cell interactions (e.g., in neurons and in other types of cells, such as Langerhans beta cells), which forms intercellular junctions by binding to beta-neurexins. It may play role in forming or maintaining synaptic junctions.
References in periodicals archive ?
So extending the assumption of X chromosome evolution from autosome we can assume that paralog of X-linked genes must be on autosome and should be involved in the same disorder; like ARHGEF6 (X chromosome) has its paralog ARHGEF3 and ARHGEF4 on autosome; similarly NLGN3, NLGN4 on X -chromosome has paralog NLGN1 and NLGN2 on autosome.