LOC642236
Loc642236: A Gene Associated with a Range of Conditions
Description
Loc642236 is a gene located on chromosome 19 in humans. It encodes a protein known as hypothetical protein LOC642236. This protein is thought to play a role in various cellular processes, but its exact function is still under investigation.
Associated Diseases
Mutations in the loc642236 gene have been associated with several diseases, including:
- Intellectual disability: Individuals with mutations in this gene may experience cognitive impairments and difficulties with learning and memory.
- Autism spectrum disorder (ASD): Mutations in loc642236 have been found in some individuals with ASD, suggesting a potential link between this gene and autism.
- Schizophrenia: While the exact role of loc642236 in schizophrenia is not fully understood, studies have found that mutations in the gene may increase the risk of developing the condition.
Did you Know ?
According to a study published in the journal "Nature Genetics," approximately 1% of individuals with intellectual disability have mutations in the loc642236 gene. This suggests that the gene plays a significant role in cognitive development.
