2 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
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14PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
visual perceptionphotoreceptor outer segmentplasma membranecone photoreceptor disc membranered-green color blindnessred color blindnessbradyopsiaTritanopia
OPN1MW2 is a medium-wave sensitive opsin functioning as a G protein-coupled photoreceptor in cone cells. Based on limited published evidence, it mediates visual perception through light absorption and phototransduction signaling in photoreceptor outer segments. Expression of opn1mw2 is developmentally regulated by thyroid hormone signaling 1 and responds to circadian and light-induced stimuli 2. The gene plays roles in visual function and circadian rhythm regulation, with alterations associated with visual system development and sleep-related responses.
1
OPN1MW2 (opn1mw2) expression is regulated by thyroid hormone signaling via MCT8; decreased expression correlates with visual system deficiencies including altered optokinetic reflex responses
PMID: 352696062
OPN1MW2 expression is involved in visual function and circadian rhythm regulation; therapeutic interventions can restore normal opn1mw2 expression to alleviate light-induced sleep disturbances
PMID: 39600360β Limited data available β This gene has 2 indexed publications. Summary and analysis may be incomplete.
red-green color blindnessOpen Targets
red color blindnessOpen Targets
blue color blindnessOpen Targets
prolonged electroretinal response suppression 2Open Targets
age-related macular degenerationOpen Targets
hyperopia, highOpen Targets
gelatinous drop-like corneal dystrophyOpen Targets
X-linked retinal dysplasiaOpen Targets
Rare isolated myopiaOpen Targets
Familial exudative vitreoretinopathyOpen Targets
Blue cone monochromatismOpen Targets
myopia 26, X-linked, female-limitedOpen Targets
retinitis pigmentosa 92Open Targets
familial pterygium of the conjunctivaOpen Targets
Pterygium of the conjunctiva, familial formOpen Targets
blue cone monochromacyOpen Targets
Progressive cone dystrophyOpen Targets
No pathogenic variants reported on ClinVar for this gene.
No tissue expression data available for this gene.