OR1L6: Difference between revisions
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Latest revision as of 20:40, 17 March 2025
OR1L6 is a gene that encodes a protein in humans. It is also known as Olfactory Receptor Family 1 Subfamily L Member 6. The OR1L6 gene is part of the olfactory receptor family, which is the largest gene family in the genome. The family members are G-protein coupled receptors that respond to smell and taste stimuli and are divided into a large number of subfamilies.
Function[edit]
The OR1L6 gene is thought to have a role in the detection of odorants. 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.
Expression[edit]
The OR1L6 gene is predominantly expressed in the olfactory epithelium. This is the thin layer of tissue, within the nasal cavity, that is responsible for detecting odors.
Clinical Significance[edit]
While the exact clinical significance of the OR1L6 gene is not fully understood, it is believed that variations in this gene may be linked to differences in individuals' sense of smell. Further research is needed to fully understand the potential clinical implications of this gene.
See Also[edit]
References[edit]
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