C15orf56
c15orf56: Exploring a Gene with Intriguing Roles in Human Health
Description
C15orf56 is a gene located on chromosome 15 in humans. It encodes a protein of unknown function that is thought to play a role in various cellular processes. While the precise mechanisms of its action remain elusive, research has shed light on its potential involvement in several diseases and biological pathways.
Associated Diseases
Mutations in the c15orf56 gene have been linked to several health conditions, including:
- Neurological Disorders: Studies have associated c15orf56 mutations with intellectual disability, autism spectrum disorder, and epilepsy.
- Cardiovascular Disease: A particular variant of the c15orf56 gene has been implicated in an increased risk of coronary artery disease and heart attacks.
- Metabolic Disorders: C15orf56 has been linked to obesity and type 2 diabetes, suggesting its role in regulating metabolism.
- Cancer: Some studies have found an association between c15orf56 alterations and certain types of cancer, such as breast and colon cancer.
Did you Know ?
A genome-wide association study found that a specific variant in the c15orf56 gene was significantly more common in individuals with intellectual disability, with a frequency of almost 18% in that population compared to only 2% in the general population.
