Homo sapiens Protein: OPN1SW | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Protein | IDBP-39988.4 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | OPN1SW | ||||||||||||||
Protein Name | opsin 1 (cone pigments), short-wave-sensitive | ||||||||||||||
Synonyms | BCP; BOP; CBT; | ||||||||||||||
Species | Homo sapiens | ||||||||||||||
Ensembl Protein | ENSP00000249389 | ||||||||||||||
InnateDB Gene | IDBG-39986 (OPN1SW) | ||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||
Function | Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal. | ||||||||||||||
Subcellular Localization | Membrane; Multi-pass membrane protein. | ||||||||||||||
Disease Associations | Tritan color blindness (CBT) [MIM:190900]: A disorder of vision characterized by a selective deficiency of blue spectral sensitivity. {ECO:0000269PubMed:1386496, ECO:0000269PubMed:1531728}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||
Tissue Specificity | The three color pigments are found in the cone photoreceptor cells. | ||||||||||||||
Comments | |||||||||||||||
Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||
PDB ID | |||||||||||||||
InterPro |
IPR000276
G protein-coupled receptor, rhodopsin-like IPR001521 Opsin, blue sensitive IPR001760 Opsin IPR017452 GPCR, rhodopsin-like, 7TM IPR019426 7TM GPCR, serpentine receptor class v (Srv) IPR019427 7TM GPCR, serpentine receptor class w (Srw) |
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PFAM |
PF00001
PF10323 PF10324 |
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PRINTS |
PR00237
PR00574 PR00238 |
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PIRSF | |||||||||||||||
SMART | |||||||||||||||
TIGRFAMs | |||||||||||||||
Post-translational Modifications | |||||||||||||||
Modification | |||||||||||||||
Cross-References | |||||||||||||||
SwissProt | P03999 | ||||||||||||||
PhosphoSite | PhosphoSite-P03999 | ||||||||||||||
TrEMBL | Q0PJU0 | ||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 611 | ||||||||||||||
UniGene | Hs.656404 | ||||||||||||||
RefSeq | NP_001699 | ||||||||||||||
HUGO | HGNC:1012 | ||||||||||||||
OMIM | 613522 | ||||||||||||||
CCDS | CCDS5806 | ||||||||||||||
HPRD | 01836 | ||||||||||||||
IMGT | |||||||||||||||
EMBL | CH236950 CH471070 DQ822478 L32835 M13295 M13296 M13297 M13298 M13299 M26172 U53874 | ||||||||||||||
GenPept | AAA35608 AAB05207 AAC51334 AAL31362 ABH01259 EAL24112 EAW83680 | ||||||||||||||