OR12D2: Difference between revisions
CSV import |
CSV import |
||
| Line 21: | Line 21: | ||
{{medicine-stub}} | {{medicine-stub}} | ||
{{No image}} | {{No image}} | ||
__NOINDEX__ | |||
Latest revision as of 20:35, 17 March 2025
OR12D2 is a gene that encodes a protein in humans. The protein is a member of the olfactory receptor family, a class of G protein-coupled receptors which are involved in the detection of smell.
Function[edit]
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. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms.
Clinical significance[edit]
While the specific function of OR12D2 is not fully understood, it is believed to play a role in the detection of smell. Mutations in this gene have been associated with a decreased sense of smell, known as anosmia. Further research is needed to fully understand the role of OR12D2 in human health and disease.
See also[edit]
References[edit]
<references />
