A search for this gene in Autworks reveals that this gene occupies a place in the largest network of genes implicated in autism, mediating inter-actions between genes responsible for the calcium channel receptors (CACNA1C, CACNA1G, CACNA1H), mutations in which are responsible for Timothy syndrome, another syndromic variant of autism [33], and a larger network of genes associated with autism through genome wide association studies (GWAS) and gene expression experiments (AR, BCL2, GRIN2A, NFKB1, among others). The gene discussed is GRIN2A; the disease is Timothy syndrome.