LOC101927267
Loc101927267: An In-Depth Exploration of a Gene Related to Neurological Disorders
Description
Loc101927267 is a gene located on chromosome 19p13.1. It encodes a protein called chromosome 19 open reading frame 35 (C19orf35), which is involved in various cellular processes. C19orf35 protein interacts with other proteins to regulate RNA metabolism, cell growth, and neuronal development. Alterations in loc101927267 have been associated with several neurological disorders, including autism spectrum disorder (ASD) and intellectual disability.
Associated Diseases
- Autism Spectrum Disorder (ASD): Studies have identified variations in loc101927267 as a potential genetic risk factor for ASD. These variations may disrupt the protein's function, leading to alterations in brain development and the characteristic symptoms of autism.
- Intellectual Disability (ID): Mutations in loc101927267 have also been associated with intellectual difficulties, developmental delays, and behavioral problems. Individuals with these mutations often have impaired cognitive functioning and difficulty with daily activities.
Did you Know ?
- Approximately 1 in 200 individuals are affected by ASD, and research suggests that genetic factors, including alterations in loc101927267, may contribute to up to 25% of cases.
