OR52E8: Difference between revisions
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Latest revision as of 20:27, 17 March 2025
OR52E8 is a gene that encodes a protein in humans. It is part of the olfactory receptor family, a group of genes that are involved in the detection of smell. The OR52E8 gene is located on chromosome 11.
Function[edit]
The OR52E8 gene is part of the olfactory receptor family, which is the largest gene family in the genome. These receptors detect odors and send signals to the brain, allowing us to perceive smells. The specific function of the OR52E8 gene is not yet fully understood, but it is believed to play a role in the detection of certain smells.
Structure[edit]
The OR52E8 gene is located on chromosome 11 and is composed of a single exon. The protein it encodes is a member of the G protein-coupled receptor superfamily. This family of proteins is characterized by a seven-transmembrane domain structure, which allows them to detect a wide range of signals and transmit them to the inside of the cell.
Clinical significance[edit]
While the specific role of the OR52E8 gene in disease is not yet fully understood, olfactory receptors in general have been implicated in a number of conditions. For example, mutations in olfactory receptor genes have been linked to anosmia, a condition characterized by a loss of the sense of smell. Further research is needed to determine the specific role of OR52E8 in disease.
See also[edit]
References[edit]
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