OR13C9: Difference between revisions
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Revision as of 04:04, 11 February 2025
OR13C9 is a protein that in humans is encoded by the OR13C9 gene. The protein is a member of the olfactory receptor family, which is involved in the detection of smell.
Function
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome.
Gene
The OR13C9 gene is located on chromosome 11, specifically 11p15.4. It spans 1,065 base pairs and encodes a protein of 315 amino acids. The gene is expressed in the olfactory epithelium, the tissue lining the nasal cavity that is involved in smell.
Clinical significance
While the exact role of OR13C9 in disease is not well understood, olfactory receptors in general have been implicated in a variety of diseases, including neurodegenerative diseases like Parkinson's disease and Alzheimer's disease, as well as cancer. Further research is needed to determine the specific role of OR13C9 in these and other conditions.
See also
References
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