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GeneE
2 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
OPN1MW2
opsin 1, medium wave sensitive 2
Chromosome X Β· Xq28
NCBI Gene: 728458Ensembl: ENSG00000166160.9HGNC: HGNC:26952UniProt: P0DN77
14PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
visual perceptionphotoreceptor outer segmentplasma membranecone photoreceptor disc membranered-green color blindnessred color blindnessbradyopsiaTritanopia
✦AI Summary

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.

Sources cited
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: 35269606
2
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: 39600360
⚠Limited data available β€” This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsβ“˜20
red-green color blindnessOpen Targets
0.15Weak
red color blindnessOpen Targets
0.10Weak
bradyopsiaOpen Targets
0.08Suggestive
blue color blindnessOpen Targets
0.08Suggestive
TritanopiaOpen Targets
0.08Suggestive
myopiaOpen Targets
0.07Suggestive
prolonged electroretinal response suppression 2Open Targets
0.07Suggestive
age-related macular degenerationOpen Targets
0.07Suggestive
hyperopia, highOpen Targets
0.07Suggestive
gelatinous drop-like corneal dystrophyOpen Targets
0.06Suggestive
X-linked retinal dysplasiaOpen Targets
0.06Suggestive
Rare isolated myopiaOpen Targets
0.06Suggestive
Familial exudative vitreoretinopathyOpen Targets
0.06Suggestive
Blue cone monochromatismOpen Targets
0.06Suggestive
myopia 26, X-linked, female-limitedOpen Targets
0.06Suggestive
retinitis pigmentosa 92Open Targets
0.06Suggestive
familial pterygium of the conjunctivaOpen Targets
0.06Suggestive
Pterygium of the conjunctiva, familial formOpen Targets
0.06Suggestive
blue cone monochromacyOpen Targets
0.05Suggestive
Progressive cone dystrophyOpen Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
OPN1MWShared pathway100%OPN1LWShared pathway100%OPN1MW3Shared pathway100%OPN1SWShared pathway75%RRHShared pathway57%RHOShared pathway50%
Tissue Expression

No tissue expression data available for this gene.

Gene Interaction Network
Click a node to explore
OPN1MW2OPN1MWOPN1LWOPN1MW3OPN1SWRRHRHO
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt P0DN77
View on AlphaFold β†—
RankingsWhere OPN1MW2 stands among ~20K protein-coding genes
  • #15,942of 20,598
    Most Researched14
Genes detectedOPN1MW2
Sources retrieved2 papers
Response timeβ€”
πŸ“„ Sources
2
1
Genetic and Neurological Deficiencies in the Visual System of
PMID: 35269606
Int J Mol Sci Β· 2022
1.00
2
Therapeutic potential of mackerel-derived peptides and the synthetic tetrapeptide TVGF for sleep disorders in a light-induced anxiety zebrafish model.
PMID: 39600360
Front Pharmacol Β· 2024
0.50