It is also important for neurite growth.[49]Neto1‐null mice have depressed LTP at Schaffer collateral‐CA1 synapses and impaired spatial learning and memory.[50] Patients with Syt1‐associated neurodevelopmental disorders demonstrate infantile hypotonia, profound intellectual disability, disordered movement, and electroencephalographic abnormalities without epilepsy or gross neuroanatomic abnormalities.[51] The gene‐concept network we generated highlighted the interplay between specific genes and their associated GO terms. This evidence concerns the gene NETO1 and epilepsy.