CCNYL1
ccnyl1: A Gene with Implications for Neurological Health
Description
The ccnyl1 gene, also known as cyclin Y-like 1, is located on chromosome 19p13.3. It encodes a protein of the same name that plays a crucial role in regulating cell cycle progression and DNA repair mechanisms. The ccnyl1 protein is particularly important for the development and maintenance of the nervous system.
Associated Diseases
Mutations in the ccnyl1 gene have been linked to several neurological disorders, including:
- Microcephaly: A condition characterized by an unusually small head and brain size.
- Intellectual disability: Difficulty with learning, problem-solving, and daily life activities.
- Autism spectrum disorder (ASD): A developmental disorder characterized by social and communication challenges.
- Epilepsy: A neurological disorder that causes seizures.
- Parkinson's disease: A neurodegenerative disorder that affects movement and coordination.
Did you Know ?
Approximately 1 in 200,000 individuals worldwide are estimated to have a mutation in the ccnyl1 gene. This makes it a relatively rare genetic disorder. However, its effects can be significant, impacting both physical and cognitive development.
