DST

Description

The DST gene, also known as the dystrophin-associated protein with a Src homology 3 domain, plays a crucial role in various biological processes, particularly in the development and function of the nervous system and skeletal muscle. It acts as a scaffolding protein, linking together different proteins within cells and regulating their activity. This interaction network is critical for maintaining cellular structure, communication, and signaling pathways. Mutations in the DST gene can lead to a range of disorders, primarily affecting the brain and muscles. Understanding the role of DST and its associated pathologies is essential for developing targeted therapies and improving patient outcomes.

Associated Diseases

• Spinal muscular atrophy (SMA)
• Amyotrophic lateral sclerosis (ALS)
• Autism spectrum disorder (ASD)
• Schizophrenia
• Intellectual disability

Did you know?

The DST gene is highly conserved across species, indicating its importance in biological function.