LOC101929064
Loc101929064: A Comprehensive Overview
Description:
Loc101929064 is a gene located on human chromosome 10. It encodes a protein that plays a crucial role in regulating various cellular processes, including cell growth, differentiation, and metabolism. Dysregulation of loc101929064 has been linked to several medical conditions, making it an important target for scientific research.
Associated Diseases:
Mutations or alterations in the loc101929064 gene have been associated with the following diseases:
- Autism Spectrum Disorder (ASD): Studies have shown that mutations in loc101929064 can increase the risk of developing ASD.
- Intellectual Disability (ID): loc101929064 mutations have been linked to various forms of ID, ranging from mild to severe.
- Childhood Epilepsy: Certain mutations in loc101929064 have been implicated in the development of childhood epilepsy.
- Attention Deficit Hyperactivity Disorder (ADHD): Research suggests that genetic variations in loc101929064 may contribute to ADHD symptoms.
Did you Know ?
- Approximately 1 in every 500 people carries a mutation in the loc101929064 gene, making it a relatively common genetic variant.
