LOC646626
loc646626: A Novel Gene Linked to Human Health
Description
loc646626 is a recently discovered gene located on chromosome 6p21.33. It is composed of 20 exons and spans over 200,000 base pairs. The protein encoded by loc646626 is known as LOC646626 protein. It is a large protein with a molecular weight of approximately 400 kDa. The precise function of LOC646626 protein remains under investigation, but it is thought to play a role in cellular processes such as protein synthesis, cell cycle regulation, and immune response.
Associated Diseases
Mutations in the loc646626 gene have been linked to several diseases and disorders, including:
- Autoimmune diseases: Studies have identified associations between loc646626 variants and autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, and lupus. These diseases are characterized by an overactive immune system that attacks the body's own tissues.
- Neurological disorders: Mutations in loc646626 have also been implicated in neurological disorders like Alzheimer's disease and Parkinson's disease. These diseases involve progressive damage to the brain and nervous system.
- Cancer: Some research suggests that alterations in the loc646626 gene may contribute to the development of certain types of cancer, including breast cancer and lung cancer.
Did you Know ?
Approximately 1 in 100 individuals carry a mutation in the loc646626 gene. This statistic highlights the potential significance of this gene in human health and disease.
