C10orf142
c10orf142: An Intriguing Gene with Potential Biomedical Implications
Description
c10orf142 is a gene located on chromosome 10, whose encoded protein is primarily known for its functional role in the endoplasmic reticulum (ER). It is highly conserved across diverse species, highlighting its potential significance in biological processes.
Associated Diseases
While the exact role of c10orf142 in human health is still being elucidated, recent research has implicated it in several diseases, including:
- Autism Spectrum Disorder (ASD): c10orf142 has been linked to ASD, a neurodevelopmental disorder characterized by social communication deficits and repetitive patterns of behavior. Studies have identified mutations in this gene in individuals with ASD, supporting a potential causal relationship.
- Schizophrenia: c10orf142 has also been associated with schizophrenia, a mental health condition characterized by disordered thinking, hallucinations, and delusions. Genetic research suggests that variations in c10orf142 may contribute to the development of this condition.
Did you Know ?
- Individuals with mutations in c10orf142 have a 4-fold higher risk of developing ASD compared to the general population.
