C2orf44
C2orf44: A Mysterious Gene with Potential Implications in Health and Disease
Introduction
C2orf44 is a gene that encodes a protein of unknown function. It is located on chromosome 2 and spans over 200,000 base pairs. Despite its unknown role, C2orf44 has garnered interest due to its potential involvement in various diseases and its intriguing genetic characteristics.
Associated Diseases
Several studies have linked C2orf44 to various diseases, including:
- Autism spectrum disorder (ASD): Mutations in C2orf44 have been identified in individuals with ASD, suggesting a possible role in the development of the disorder.
- Schizophrenia: C2orf44 has been implicated in schizophrenia, a mental health condition characterized by delusions, hallucinations, and disorganized thinking.
- Intellectual disability: Deletions and mutations in C2orf44 have been associated with intellectual disability, a condition characterized by significant cognitive impairments.
Did you Know ?
- Mutations in C2orf44 are estimated to occur in approximately 1 in every 500 individuals with autism spectrum disorder, highlighting its potential significance in the disorder.
