Target intelligence / Profile preview

Olfactory receptor family 6 subfamily M member 2 pseudogene (OR6M2P)

Target
OR6M2P
Molecular classification
Pseudogene (primary), Olfactory receptor superfamily (as origin), 7-transmembrane G protein-coupled receptor (ancestral/class, but not active)
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Overview

Olfactory receptor family 6 subfamily M member 2 pseudogene is a non-functional genomic sequence in humans, classified as a pseudogene derived from the olfactory receptor gene family[3][9]. Olfactory receptors generally mediate the detection of odorants via G protein-coupled mechanisms in the nose, but pseudogenes like OR6M2P do not encode functional olfactory receptor proteins and are presumed to have no role in odorant detection or signal transduction[7][9]. Pseudogenes typically arise through mutations that disrupt the coding sequence, such as frameshifts or premature stop codons, and are considered "genomic fossils"; however, some pseudogenes in the olfactory receptor family can unexpectedly retain regulatory function or even encode rare active proteins through translational readthrough[4][5]. For OR6M2P, there is currently no evidence of protein expression or function, and it is annotated as a molecularly inactive pseudogene[3][4][9]. Note: While some pseudogenes in olfactory receptor families can display rare non-canonical activities (such as unexpected functional protein via translational readthrough, as observed in some insect species—not described for human OR6M2P), this does not apply for the canonical human OR6M2P[4][5].

Other names
OR6M2POlfactory receptor, family 6, subfamily M, member 2 pseudogene
02

Mechanism of action

Not applicable; pseudogenes do not encode active proteins that can be targeted

03

Biological functions

None known; pseudogenes are generally non-functional in terms of encoding active proteinsOccasional regulatory roles as RNA in some pseudogenes (not specifically reported for OR6M2P)
04

Disease associations

None establishedOlfactory receptor pseudogenes generally do not have disease associations unless re-expressed abnormally or if transcript has regulatory function

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