LOC102724663
Loc102724663: An Unraveling Enigma in the Realm of Genetics
Description
Loc102724663, also known as C16orf97, is a gene located on chromosome 16 in humans. It encodes a protein of unknown function, though research suggests its involvement in various cellular processes, including cell growth, differentiation, and apoptosis.
Associated Diseases
Mutations in Loc102724663 have been linked to several genetic disorders, including:
- Microcephaly: A condition characterized by an abnormally small head and brain.
- Developmental delay: Delays in reaching developmental milestones, such as sitting, walking, or talking.
- Intellectual disability: Difficulties in cognitive functions, such as learning, reasoning, and problem-solving.
- Autism spectrum disorder (ASD): A neurodevelopmental condition that affects communication, social interaction, and repetitive behaviors.
Did you Know ?
As of 2021, mutations in Loc102724663 have been identified in approximately 1 in every 20,000 individuals. However, it is believed that these mutations are underdiagnosed, as many cases may be missed due to their rarity.
