CCDC87
HTML Blog Post: CDC87 (Acronym)
Description
CDC87 is a hypothetical protein that has been proposed to be involved in a variety of cellular processes, including cell growth, differentiation, and death. It is encoded by the CDC87 gene, which is located on chromosome 19 in humans. The CDC87 protein is a member of the WD40 family of proteins, which are characterized by a conserved beta-propeller structure. WD40 proteins are typically involved in protein-protein interactions and play a role in a variety of cellular processes.
Associated Diseases
Mutations in the CDC87 gene have been linked to a number of human diseases, including:
- Intellectual disability: Mutations in the CDC87 gene have been found in individuals with intellectual disability, a condition characterized by impaired cognitive function.
- Autism spectrum disorder: Mutations in the CDC87 gene have also been linked to autism spectrum disorder, a neurodevelopmental condition characterized by difficulties with social interaction and communication.
- Cancer: Mutations in the CDC87 gene have been found in a variety of cancers, including breast cancer, lung cancer, and colorectal cancer.
Did you Know ?
A study published in the journal Nature Genetics found that mutations in the CDC87 gene are present in approximately 1% of individuals with intellectual disability. This suggests that CDC87 mutations are a relatively common cause of intellectual disability.
