OR1L8

OR1L8 is a gene that encodes a protein in humans. It is also known as Olfactory Receptor Family 1 Subfamily L Member 8. This gene is part of the olfactory receptor family, which is the largest gene family in the genome. The olfactory receptors are G protein-coupled receptors that are involved in the detection of smell.

Function

The OR1L8 gene is expressed in the olfactory epithelium, where it is involved in the detection of odor molecules. The protein encoded by this gene is a member of the olfactory receptor family, and it is believed to play a role in the perception of smell. The exact function of this gene is not fully understood, but it is thought to be involved in the detection of specific odor molecules.

Structure

The OR1L8 gene is located on chromosome 1, and it spans approximately 1 kilobase. The gene contains two exons and one intron. The protein encoded by this gene is a seven-transmembrane domain protein, which is characteristic of G protein-coupled receptors.

Clinical Significance

While the exact role of OR1L8 in disease is not fully understood, it is thought that mutations in this gene may be associated with certain disorders of smell, such as anosmia. Further research is needed to fully understand the clinical significance of this gene.

See Also

• Olfactory receptor
• Anosmia
• G protein-coupled receptor