DMRTC1
Description
The DMRTC1 (DMRT like family C1) is a protein-coding gene located on chromosome X.
DMRTC1 is a gene located on chromosome 16. It encodes a protein that is involved in the development of the nervous system. It is believed to play a role in the formation of synapses, which are the junctions between nerve cells. Mutations in DMRTC1 have been associated with autism spectrum disorder and intellectual disability.
DMRTC1 is a gene that encodes a protein that plays a role in the development of the nervous system. It is involved in the formation of synapses, which are the junctions between nerve cells. Mutations in DMRTC1 have been associated with autism spectrum disorder and intellectual disability.
DMRTC1 is also known as -.
