C1orf194
c1orf194: An Emerging Gene of Intriguing Significance
Description:
c1orf194 (chromosome 1 open reading frame 194) is an enigmatic gene located on chromosome 1. Its function and biological role remain largely elusive, but recent research has shed light on its potential involvement in various diseases and cellular processes.
Associated Diseases:
While the precise disease mechanisms are still being explored, c1orf194 has been associated with several conditions:
- Microcephaly: A rare congenital disorder characterized by an unusually small head circumference.
- Intellectual disability: A condition affecting cognitive abilities, such as learning and problem-solving.
- Autism spectrum disorder: A neurodevelopmental disorder that impairs social communication and interaction.
- Schizophrenia: A severe mental illness that affects thoughts, emotions, and behavior.
- Cancer: Studies have suggested that c1orf194 may play a role in the development and progression of certain types of cancer, including breast and lung cancer.
Did you Know ?
About 1 in every 10,000 individuals carries a mutation in the c1orf194 gene. This highlights the potential impact of this gene on human health and underscores the need for further research.