LOC441178
Description
Loc441178: A Gene Linked to Autism Spectrum Disorder
Loc441178 is a gene located on the X chromosome. It is involved in the production of a protein called KIAA1267, which plays a role in the development and function of the brain. Mutations in the loc441178 gene have been linked to autism spectrum disorder (ASD), a neurodevelopmental condition that affects social interaction, communication, and behavior.
Associated Diseases
Mutations in the loc441178 gene have been primarily associated with autism spectrum disorder (ASD). ASD is a complex and heterogeneous condition, and the specific symptoms and severity can vary greatly from person to person. Common symptoms of ASD include:
- Social difficulties, such as challenges with making eye contact, interacting with others, and understanding social cues
- Communication problems, such as difficulty with verbal and nonverbal language
- Restricted and repetitive interests and behaviors, such as intense focus on specific topics or repetitive movements
- Sensory sensitivities, such as over- or under-sensitivity to light, sound, or touch
Did you Know ?
According to the Centers for Disease Control and Prevention (CDC), the prevalence of ASD in the United States is estimated to be 1 in 44 children. This means that approximately 2% of children in the U.S. have ASD. ASD is more common in boys than girls, with a ratio of about 4:1.
