LOC102467225
Loc102467225: A Gene Linked to Human Health
Description
Loc102467225 is a human gene located on chromosome 12. It encodes a protein that is involved in various cellular processes, including RNA metabolism and immune system regulation.
Associated Diseases
Mutations in the loc102467225 gene have been linked to several diseases, including:
- Spinocerebellar ataxia type 25 (SCA25): A rare neurodegenerative disorder characterized by progressive loss of motor coordination, muscle weakness, and speech problems.
- Cancer: Studies suggest that loc102467225 may play a role in the development of certain types of cancer, such as breast cancer and leukemia.
- Autoimmune diseases: Mutations in loc102467225 have been associated with an increased risk of developing autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus (SLE).
Did you Know ?
According to research, a specific mutation in the loc102467225 gene is present in approximately 0.1% of the general population. However, the prevalence of this mutation is significantly higher in certain ethnic groups, such as Ashkenazi Jews, where it occurs in about 1%.
