OR10G8: Difference between revisions

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Latest revision as of 20:34, 17 March 2025

OR10G8 is a gene that encodes a protein in humans. It is also known as Olfactory Receptor Family 10 Subfamily G 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 play a role in the detection of smell.

Function[edit]

The OR10G8 gene is a member of the olfactory receptor genes family. 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]

OR10G8 is expressed in the olfactory epithelium, where it is involved in the detection of odorants. The specific function of this protein has not yet been determined; however, it may play a role in the perception of odorants in the olfactory epithelium.

Clinical Significance[edit]

While the specific clinical significance of OR10G8 is not yet fully understood, mutations in olfactory receptor genes, including OR10G8, have been associated with various diseases. For example, a decreased sense of smell (anosmia) can be caused by mutations in olfactory receptor genes.

See Also[edit]

References[edit]

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