OR3A1: Difference between revisions
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Revision as of 00:22, 11 February 2025
OR3A1 is a gene that encodes a protein in the olfactory receptor family. This family is a group of G protein-coupled receptors that are involved in the detection of smell. The OR3A1 gene is specifically involved in the detection of certain odors.
Function
The OR3A1 gene is part of the olfactory receptor family, which is responsible for the detection of odors. These receptors are located in the olfactory epithelium, a specialized tissue inside the nose that detects smells. When an odor molecule binds to an olfactory receptor, it triggers a signal that is sent to the brain, allowing us to perceive the smell.
Structure
The OR3A1 gene is located on chromosome 17 and is composed of one exon. The protein it encodes, OR3A1, is a member of the rhodopsin-like receptors subfamily. Like all G protein-coupled receptors, OR3A1 has seven transmembrane domains, which allow it to span the cell membrane and interact with both the inside and outside of the cell.
Clinical significance
Mutations in the OR3A1 gene have been associated with a reduced ability to smell certain odors. This can lead to a condition known as anosmia, which is the inability to perceive smell. However, more research is needed to fully understand the role of OR3A1 in smell perception and anosmia.
See also
References
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