OR1A2: Difference between revisions

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Latest revision as of 20:21, 17 March 2025

OR1A2 is a gene that encodes the olfactory receptor 1A2 protein in humans. The olfactory receptor family is the largest in the genome, with members located on almost all human chromosomes.

Function[edit]

The olfactory system is a sensory system used for the sense of smell (olfaction). Olfactory receptors, such as OR1A2, are proteins that bind odor molecules resulting in a neuronal response which allows the perception of smell. These receptors are expressed in the cilia of the olfactory sensory neurons.

Gene[edit]

The OR1A2 gene is located on chromosome 11, specifically at 11p15.4. It spans approximately 1 kilobase and consists of a single coding exon. The OR1A2 gene is a member of the olfactory receptor family, and is part of the 1A subfamily.

Protein Structure[edit]

The OR1A2 protein is a member of the class A rhodopsin-like family of G protein-coupled receptors. It is composed of 312 amino acids and has a molecular weight of approximately 35 kDa. The protein has seven transmembrane domains, a characteristic feature of G protein-coupled receptors.

Clinical Significance[edit]

Variations in the OR1A2 gene have been associated with differences in the sense of smell. Certain single nucleotide polymorphisms (SNPs) in this gene have been linked to a heightened sensitivity to certain odors.

See Also[edit]

References[edit]

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