NPB
Description
The NPB gene, located on chromosome 17, encodes a protein essential for normal neurodevelopment. It plays a crucial role in the formation and function of synapses, the junctions between nerve cells. Mutations in NPB can disrupt these processes, leading to a range of neurological disorders. The NPB protein interacts with other proteins involved in neuronal signaling and plasticity, contributing to the complex regulation of brain function.
Associated Diseases
Did you know?
Studies have shown that variations in the NPB gene are associated with differences in cognitive abilities, including verbal fluency and memory.
