LOC388882
Loc388882: An Enigmatic Gene with Complex Implications
Description:
Loc388882 is a mysterious gene located on chromosome 16p13. It is responsible for encoding a protein of unknown function and has been implicated in various diseases and disorders.
Associated Diseases:
- Colorectal cancer: Loc388882 has been found to be overexpressed in colorectal cancer cells, suggesting its potential role in tumor growth and progression.
- Breast cancer: Studies have indicated a correlation between Loc388882 expression and increased risk of breast cancer.
- Pulmonary hypertension: Abnormal expression of Loc388882 has been associated with the development of pulmonary hypertension, a condition characterized by elevated blood pressure in the arteries of the lungs.
- Intellectual disability: Mutations in Loc388882 have been linked to certain forms of intellectual disability, particularly in individuals with chromosomal abnormalities.
Did you Know ?
- Studies have shown that a specific variant of Loc388882 is associated with a significantly increased risk (up to 40%) of developing colorectal cancer.
