C6orf165
c6orf165: An Enigma in Genetic Research
Description
c6orf165 (chromosome 6 open reading frame 165) is a gene located on the long arm of chromosome 6. It encodes a protein of unknown function, consisting of 461 amino acids. Analysis of its amino acid sequence suggests it may interact with other proteins, but its precise role in cellular processes remains elusive.
Associated Diseases
The involvement of c6orf165 in human diseases is still poorly understood. However, genome-wide association studies have implicated variations within this gene with several conditions:
- Schizophrenia: Researchers have identified associations between specific c6orf165 mutations and an increased risk of developing schizophrenia.
- Autism Spectrum Disorder (ASD): Variations in c6orf165 have also been linked to an increased susceptibility to ASD.
- Other Neurodevelopmental Disorders: Ongoing research is exploring the role of c6orf165 in other neurodevelopmental disorders, such as attention deficit hyperactivity disorder (ADHD) and intellectual disability.
Did you Know ?
According to the National Institute of Health's PubMed database, as of October 2023, there have been only 42 published scientific articles that mention c6orf165. This highlights the limited knowledge and ongoing research surrounding this gene.
