OPN1LW G338E [photoreceptor disc membrane]

Stable Identifier
R-HSA-2471646
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
photoreceptor disc membrane
Synonyms
Red-sensitive opsin, OPSR_HUMAN, OPN1LW
Icon
OPN1LW G338E [photoreceptor disc membrane] icon
OPN1LW G338E [photoreceptor disc membrane] icon
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:P04000 OPN1LW
Gene Names
OPN1LW, RCP
Chain
chain:1-364
Reference Genes
BioGPS Gene:5956 OPN1LW
COSMIC (genes):OPN1LW OPN1LW
CTD Gene:5956 OPN1LW
dbSNP Gene:5956 OPN1LW
ENSEMBL:ENSG00000102076 OPN1LW
HGNC:9936 OPN1LW
KEGG:hsa:5956 OPN1LW
Monarch:5956 OPN1LW
NCBI Gene:5956 OPN1LW
OMIM:300822 OPN1LW
UCSC:P04000 OPN1LW
Reference Transcript
Other Identifiers
11735456_s_at
17108234
17108244
17108254
221327_3p_s_at
221327_PM_s_at
221327_s_at
3996145
3996146
3996147
3996148
3996149
3996151
3996152
3996153
3996154
3996157
3996158
3996174
3996175
3996177
3996178
3996179
3996180
3996181
3996182
3996184
3996185
3996202
3996203
3996205
3996208
3996209
3996211
3996212
3996215
3996216
5956
8170811
8170816
8170825
A_23_P96623
GE567795
GO:0001750
GO:0004930
GO:0005515
GO:0005886
GO:0007165
GO:0007186
GO:0007601
GO:0007602
GO:0008020
GO:0009584
GO:0009881
GO:0016020
GO:0032467
GO:0050877
GO:0060089
GO:0071482
GO:0097381
HMNXSV003040100
ILMN_1677153
K03494_s_at
PH_hs_0034119
TC0X000764.hg
TC0X000765.hg
TC0X000766.hg
TC0X001932.hg
TC0X001934.hg
Z68193_at
g4503964_3p_s_at
Participates
as a member of
Other forms of this molecule
OPN1LW P307L [photoreceptor disc membrane]
OPN1LW C203R [photoreceptor disc membrane]
OPN1LW R247* [photoreceptor disc membrane]
11cRAL-OPN1LW [photoreceptor disc membrane]
at-retinyl-OPN1LW [photoreceptor disc membrane]
OPN1LW [photoreceptor disc membrane]
Modified Residues
Name
glycine 338 replaced with L-glutamic acid
Coordinate
338
PsiMod
glycine removal [MOD:01638]
A protein modification that effectively removes or replaces an glycine.
L-glutamic acid residue [MOD:00015]
A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.
Disease
Name Identifier Synonyms
red color blindness DOID:13910 Protanopia, Protan defect (disorder), Protan defect
Cross References
Guide to Pharmacology - Targets
ENSEMBL
OpenTargets
HPA
PRO
Pharos - Targets
GlyGen
Orphanet
PDB
Interactors (2)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q8IXM6 NRM      0.556 3
 UniProt:A5PKU2 A5PKU2      0.556 3
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