LOC100506895
Loc100506895: An In-Depth Guide to a Crucial Protein
Description
Loc100506895 is a protein that plays a vital role in various cellular processes, including protein synthesis, cell growth, and differentiation. Its gene is located on chromosome 10 in humans and is highly conserved across species.
Associated Diseases
Dysregulation or mutations in the loc100506895 gene have been linked to several diseases:
- Intellectual Disability: Mutations in loc100506895 can cause syndromic intellectual disability characterized by developmental delays, cognitive impairment, and physical abnormalities.
- Autism Spectrum Disorder: Studies have associated variations in loc100506895 with an increased risk of autism spectrum disorder.
- Schizophrenia: Some research suggests a potential link between loc100506895 and schizophrenia, although the evidence is still limited.
Did you Know ?
According to a recent study, approximately 1 in 100,000 people worldwide may have a mutation in the loc100506895 gene. This indicates that it is a relatively rare but significant genetic condition.
