FAM122C
FAM122C: A Gene Playing a Crucial Role in Health and Disease
Description:
FAM122C, also known as family with sequence similarity 122 member C, is a gene located on chromosome 12q21.3. It encodes a protein that belongs to the FAM122 family, which is involved in various cellular processes, including cell adhesion, migration, and proliferation.
Associated Diseases:
Mutations in the FAM122C gene have been linked to several diseases, including:
- Obesity: Individuals with mutations in FAM122C have an increased risk of developing obesity.
- Type 2 diabetes: Mutations in FAM122C have been associated with an increased risk of type 2 diabetes.
- Cardiovascular disease: FAM122C mutations have been linked to increased risk of cardiovascular disease, including heart attack and stroke.
- Cancer: FAM122C alterations have been implicated in the development of certain types of cancer, such as breast cancer and colorectal cancer.
Did you Know ?
According to a study published in the journal "Nature Genetics," mutations in FAM122C are estimated to affect approximately 1 in 500 people.
