OR3A1: Difference between revisions
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Latest revision as of 20:26, 17 March 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[edit]
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[edit]
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[edit]
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[edit]
References[edit]
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