LOC101929596
Description
Loc101929596 is a protein-coding gene located on chromosome 10q24.31. It encodes a protein of 419 amino acids that is involved in various cellular processes, including cell growth, differentiation, and apoptosis.
Associated Diseases
Mutations in the loc101929596 gene have been associated with several diseases, including:
- Intellectual disability: Mutations in loc101929596 have been implicated in intellectual disability, a condition characterized by significant limitations in intellectual functioning and adaptive behavior.
- Developmental delay: Loc101929596 mutations can also lead to developmental delay, a condition where a child's development is significantly slower than expected in one or more areas, such as language, motor skills, or social interactions.
- Autism spectrum disorder (ASD): Some studies have found an association between loc101929596 mutations and ASD, a neurodevelopmental disorder characterized by social and communication difficulties, as well as repetitive behaviors.
- Schizophrenia: Loc101929596 mutations have also been linked to schizophrenia, a severe mental illness that affects a person's thoughts, feelings, and behavior.
Did you Know ?
- Approximately 1 in 500,000 people worldwide may have a mutation in the loc101929596 gene.
