DSCR9
Description
The DSCR9 (Down syndrome critical region 9) is a ncRNA gene located on chromosome 21.
The DSCR9 gene is located on chromosome 21 and is thought to be involved in the development of Down syndrome. Mutations in the DSCR9 gene have been linked to a number of neurological disorders, including Alzheimer's disease, autism spectrum disorder, and epilepsy.
The DSCR9 gene encodes a protein that is thought to play a role in regulating neuronal calcium signaling, synaptic plasticity, and cognitive function. It may also be involved in the development of the brain and the regulation of cell growth and survival.
DSCR9 is also known as NCRNA00038.