WP5398 - NRXN1 deletion syndrome - Homo sapiens
收藏NIAID Data Ecosystem2026-05-02 收录
下载链接：
https://www.ndexbio.org/viewer/networks/451af032-1439-11f0-9806-005056ae3c32
下载链接
链接失效反馈官方服务：
资源简介：
Mutations or loss of the NRXN1 gene, located on chromosome 2, is associated with severe brain disorders, autism, schizophrenia, and developmental delay. NRXN1 binds to neurolignins bridging the synaptic cleft. Alternatively spliced NRXN1 and NRXN3 influence the expression of NMDA and AMPA receptors.
创建时间：
2025-04-17
