OR2L2: Difference between revisions
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Revision as of 04:33, 11 February 2025
OR2L2 is a gene that encodes the olfactory receptor, family 2, subfamily L, member 2 protein in humans. The olfactory receptor proteins are members of a large family of G-protein coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome.
Function
The protein encoded by the OR2L2 gene is an olfactory receptor. 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.
Gene
The OR2L2 gene is located on the chromosome 1 (1q44). The gene spans approximately 1.1 kb and consists of 1 exon. The OR2L2 gene produces a mRNA molecule of approximately 1.1 kb in size.
Clinical Significance
While the specific clinical significance of OR2L2 is not yet fully understood, olfactory receptors in general are thought to have roles in various human diseases such as cancer, metabolic and neurological diseases.
See Also
References
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