C1orf111
Uncovering the Enigmatic c1orf111: A Gene Linked to Brain Function and Disease
Description
c1orf111 is a gene located on chromosome 1 in humans. It encodes a protein of unknown function, but recent research has shed light on its potential role in cognition and neurodegenerative diseases.
Associated Diseases
Mutations in c1orf111 have been linked to several neurological disorders, including:
- Intellectual disability: Individuals with mutations in c1orf111 often exhibit cognitive impairments, developmental delays, and behavioral problems.
- Autism spectrum disorder (ASD): Studies have identified an association between c1orf111 mutations and increased risk of ASD.
- Schizophrenia: Recent research suggests that c1orf111 mutations may also play a role in the development of schizophrenia.
Did you Know ?
Approximately 1 in 500 people carry a mutation in the c1orf111 gene, making it a relatively common genetic variation.
