C11orf65
Unraveling the Enigma of c11orf65: A Comprehensive Guide
Description
c11orf65 (chromosome 11 open reading frame 65) is a captivating gene found on chromosome 11. This mysterious gene has remained shrouded in enigma, but recent research has begun to shed light on its intricate nature. It encodes a protein of unknown function, leaving scientists curious about its role in human biology and disease.
Associated Diseases
While the precise mechanisms of c11orf65 are still uncertain, its involvement in various diseases has been hinted at:
- Autism Spectrum Disorder (ASD): Studies have identified genetic variations in c11orf65 in individuals with ASD, suggesting a potential role in the development of this neurodevelopmental condition.
- Intellectual Disability (ID): Similar genetic associations have been observed in individuals with ID, further strengthening the connection between c11orf65 and cognitive impairments.
- Neurodevelopmental Disorders: The potential impact of c11orf65 on neurodevelopment extends beyond specific conditions, encompassing a broader spectrum of developmental challenges.
Did you Know ?
One in 150 individuals may carry genetic mutations in c11orf65. This startling statistic highlights the potential prevalence of this gene‘s influence on human health and raises questions about its role in a wider population.
