OR10G7: Difference between revisions

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Latest revision as of 20:19, 17 March 2025

OR10G7 is a gene that encodes a protein in humans. It is also known as Olfactory Receptor Family 10 Subfamily G Member 7. 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 OR10G7 gene is a member of the olfactory receptor genes family. These genes are expressed in the olfactory epithelium of the nose and are involved in the detection of volatile odorant molecules. The OR10G7 gene encodes a protein that is thought to be involved in the perception of smell. However, the specific function of this gene is not yet fully understood.

Structure[edit]

The OR10G7 gene is located on chromosome 1, specifically on the long (q) arm at position 23.2. The gene spans approximately 1,000 base pairs of DNA. Like other olfactory receptor genes, OR10G7 consists of a single coding exon.

Clinical Significance[edit]

While the specific function of OR10G7 is not yet fully understood, it is thought that mutations in this gene may be associated with a decreased sense of smell, known as anosmia. Further research is needed to confirm this association and to understand the potential implications for human health.

See Also[edit]

References[edit]

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