C17orf102
c17orf102: A Gene Linked to Neurodevelopment and Obesity
Introduction
c17orf102 (also known as LOC101929381 or C17ORF102) is a gene located on chromosome 17 of the human genome. It encodes a protein of unknown function that is thought to play a role in neurodevelopment and metabolism. Researchers are still studying the gene's precise function and its role in human health.
Associated Diseases
Mutations in c17orf102 have been associated with several neurodevelopmental and metabolic conditions, including:
- Intellectual disability: Mutations in c17orf102 have been linked to intellectual disabilities, ranging from mild to severe.
- Autism spectrum disorder: Some studies have suggested an association between c17orf102 mutations and autism spectrum disorder (ASD).
- Schizophrenia: A small number of studies have found an increased risk of schizophrenia in individuals with c17orf102 mutations.
- Obesity: Mutations in c17orf102 have also been linked to an increased risk of obesity in children and adults.
Did you Know ?
A recent study found that approximately 1 in 100,000 individuals worldwide have a mutation in the c17orf102 gene. This suggests that the gene plays a significant role in human health.
