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MIRAGE
Long-wave-sensitive opsin 1
Summary
- UniProt ID
- P04000
- Gene Symbol
-
- OPN1LW
- RCP
- Gene ID
- 5956
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Disease variant
- Disulfide bond
- G-protein coupled receptor
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Retinal protein
- Transmembrane helix
- Vision
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| photoreceptor disc membrane |
| photoreceptor outer segment |
| GO Term |
|---|
| G protein-coupled photoreceptor activity |
| photoreceptor activity |
Sequence
MAQQWSLQRLAGRHPQDSYEDSTQSSIFTYTNSNSTRGPFEGPNYHIAPRWVYHLTSVWMIFVVTASVFTNGLVLAATMKFKKLRHPLNWILVNLAVADLAETVIASTISIVNQVSGYFVLGHPMCVLEGYTVSLCGITGLWSLAIISWERWMVVCKPFGNVRFDAKLAIVGIAFSWIWAAVWTAPPIFGWSRYWPHGLKTSCGPDVFSGSSYPGVQSYMIVLMVTCCIIPLAIIMLCYLQVWLAIRAVAKQQKESESTQKAEKEVTRMVVVMIFAYCVCWGPYTFFACFAAANPGYAFHPLMAALPAYFAKSATIYNPVIYVFMNRQFRNCILQLFGKKVDDGSELSSASKTEVSSVSSVSPA
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Defective visual phototransduction due to OPN1LW loss of function | Homo sapiens |
| G alpha (i) signalling events | Homo sapiens |
| Opsins | Homo sapiens |
| The retinoid cycle in cones (daylight vision) | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050679 | blue cone monochromacy | |
| DOID:13910 | red color blindness |
