C14orf177
C14orf177: An Intriguing Gene Linked to Autism Spectrum Disorder
Description
C14orf177 is a gene located on chromosome 14 in humans. It encodes a protein of unknown function, but its unique characteristics have made it a subject of intense research, particularly in relation to autism spectrum disorder (ASD).
Associated Diseases
C14orf177 has been strongly associated with ASD, a neurodevelopmental disorder characterized by difficulties in social interaction, communication, and repetitive behaviors. Studies have found that individuals with ASD have an increased likelihood of having mutations or variations in the C14orf177 gene.
Did you Know ?
A large-scale study published in 2019 found that mutations or variations in C14orf177 were present in approximately 1% of children with ASD. This suggests that C14orf177 plays a significant role in the development of this disorder.
