C12orf10
c12orf10: An Intriguing Gene with Connections to Health and Disease
Description
c12orf10, also known as chromosome 12 open reading frame 10, is a gene found on chromosome 12 in humans. It encodes a protein of unknown function. Recent research suggests that c12orf10 may play a role in various biological processes, including cell growth, differentiation, and metabolism.
Associated Diseases
Despite its unknown function, c12orf10 has been linked to several diseases, including:
- Cancer: Studies have associated increased c12orf10 expression with poor prognosis in certain types of cancer, such as lung, colorectal, and breast cancer.
- Cardiovascular disease: Variations in c12orf10 have been associated with an increased risk of heart failure and coronary artery disease.
- Neurological disorders: Alterations in c12orf10 have been implicated in neurological conditions, such as Alzheimer's disease and schizophrenia.
Did you Know ?
A study published in the journal "Nature Genetics" found that a specific genetic variant in c12orf10 is associated with a 7% increase in the risk of developing type 2 diabetes.
