C19ORF12 : chromosome 19 open reading frame 12
Description
C19ORF12, located on chromosome 19, is a gene that encodes a protein of unknown function. Despite its elusive role, recent research suggests its potential involvement in several physiological processes, particularly in the nervous system and immune response. Studies have linked C19ORF12 variations to neurological disorders and autoimmune diseases, highlighting its potential as a therapeutic target. Further investigation is needed to fully understand its molecular mechanisms and clinical significance.
Associated Diseases
- Neurological Disorders (e.g., Alzheimer‘s Disease, Parkinson‘s Disease, Amyotrophic Lateral Sclerosis)
- Autoimmune Diseases (e.g., Rheumatoid Arthritis, Systemic Lupus Erythematosus)
- Cancer (e.g., Lung Cancer, Colorectal Cancer)
- Infectious Diseases (e.g., Viral Infections, Bacterial Infections)
Did you know?
C19ORF12 is a highly conserved gene across different species, suggesting its importance in fundamental biological processes.
