DPY19L2 : dpy-19 like 2
Description
DPY19L2, also known as DYF-19L2, is a gene that encodes a protein involved in various cellular functions, including DNA replication, cell division, and DNA repair. The protein interacts with other proteins, forming complexes essential for maintaining genomic stability and proper cell function. Mutations in this gene can lead to various genetic disorders, highlighting its importance in human health.
Associated Diseases
- Microcephalic primordial dwarfism type II
- Autosomal recessive cerebellar ataxia
- Intellectual disability
- Hypomyelination
- Spinal muscular atrophy
Did you know?
DPY19L2 was initially discovered in a genetic screen for mutations affecting the development of the nematode worm Caenorhabditis elegans, highlighting its conserved role in various organisms.
