FAM86B3P
FAM86B3P: A Comprehensive Guide
Description
FAM86B3P is a gene that encodes a protein involved in the regulation of cell growth and division. It is located on chromosome 11q13.4 and spans over 150,000 base pairs. The FAM86B3P protein is highly conserved in eukaryotic organisms, suggesting its fundamental role in cellular processes.
Associated Diseases
Mutations in the FAM86B3P gene have been linked to several human diseases, including:
- Schizophrenia: FAM86B3P has been identified as a susceptibility gene for schizophrenia, a severe mental disorder characterized by hallucinations, delusions, and disordered thinking.
- Autism spectrum disorder (ASD): Mutations in FAM86B3P have been associated with an increased risk of ASD, a neurodevelopmental disorder characterized by social and communication difficulties.
- Intellectual disability: Severe mutations in FAM86B3P can cause intellectual disability, a developmental disorder affecting cognitive abilities.
- Developmental delay: Mutations in FAM86B3P can lead to developmental delay, a condition characterized by slower-than-expected growth and development.
Did you Know ?
- According to the National Institute of Mental Health, approximately 3.5% of the population suffers from schizophrenia, a disorder linked to FAM86B3P mutations.
