LOC101929524
Loc101929524: An Intriguing Human Gene and Its Biological Significance
Description
Loc101929524, also known as C15orf67, is a gene located on chromosome 15 in humans. It is composed of 12 exons and encodes a protein of 556 amino acids. The primary function of the Loc101929524 protein remains largely unknown, but it has been linked to various biological processes and diseases.
Associated Diseases
Mutations in the Loc101929524 gene have been associated with a range of diseases, including:
- Intellectual disability: Some individuals with intellectual disability have been found to carry mutations in the Loc101929524 gene.
- Autism spectrum disorder (ASD): Studies have suggested that variations in the Loc101929524 gene may contribute to the development of ASD.
- Mitochondrial disorders: Loc101929524 has been implicated in mitochondrial dysfunction, which can lead to a group of disorders that affect energy production in the body.
- Kidney disease: Mutations in Loc101929524 have been linked to polycystic kidney disease, a condition characterized by the formation of cysts in the kidneys.
Did you Know ?
According to the National Library of Medicine's Genetics Home Reference, mutations in the Loc101929524 gene account for approximately 1% of cases of intellectual disability.
