FAM231D
Title: FAM231D: A Comprehensive Overview
Description:
FAM231D is a gene that encodes a protein known as family with sequence similarity 231, member D. This protein plays a crucial role in several cellular processes, including cell growth, proliferation, and differentiation. Mutations in the FAM231D gene have been linked to various diseases, including intellectual disability, autism spectrum disorder, and certain types of cancer.
Associated Diseases:
- Intellectual disability
- Autism spectrum disorder
- Schizophrenia
- Obsessive-compulsive disorder
- Bipolar disorder
- Prostate cancer
- Lung cancer
Did you Know ?
Mutations in the FAM231D gene are estimated to occur in approximately 1 in 100,000 people, making it a relatively rare genetic condition. However, these mutations can have a significant impact on the health and well-being of individuals who carry them.
