Version 5.4
| Mus musculus Gene: Opn1sw | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Summary | |||||||||
| InnateDB Gene | IDBG-131195.6 | ||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||
| Gene Symbol | Opn1sw | ||||||||
| Gene Name | opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan) | ||||||||
| Synonyms | AW551857; Bcp | ||||||||
| Species | Mus musculus | ||||||||
| Ensembl Gene | ENSMUSG00000058831 | ||||||||
| Encoded Proteins |
opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
|
||||||||
| Protein Structure | |||||||||
| Useful resources | Stemformatics EHFPI ImmGen | ||||||||
| Entrez Gene | |||||||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000128617:
This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008] |
||||||||
| Gene Information | |||||||||
| Type | Protein coding | ||||||||
| Genomic Location | Chromosome 6:29376671-29388468 | ||||||||
| Strand | Reverse strand | ||||||||
| Band | A3.3 | ||||||||
| Transcripts |
|
||||||||
| Interactions | |||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
|
||||||||
| Gene Ontology | |||||||||
Molecular Function |
|
||||||||
| Biological Process |
|
||||||||
| Cellular Component |
|
||||||||
| Orthologs | |||||||||
|
Species
Homo sapiens
Bos taurus
|
Gene ID
Gene Order
Not yet available
|
||||||||
| Pathways | |||||||||
| NETPATH | |||||||||
| REACTOME |
GPCR downstream signaling pathway
Disease pathway
Signaling by GPCR pathway
Class A/1 (Rhodopsin-like receptors) pathway
Opsins pathway
GPCR ligand binding pathway
G alpha (i) signalling events pathway
Visual phototransduction pathway
Retinoid cycle disease events pathway
The retinoid cycle in cones (daylight vision) pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
|
||||||||
| KEGG | |||||||||
| INOH | |||||||||
| PID NCI | |||||||||
| Pathway Predictions based on Human Orthology Data | |||||||||
| NETPATH | |||||||||
| REACTOME |
G alpha (i) signalling events pathway
Opsins pathway
Class A/1 (Rhodopsin-like receptors) pathway
The retinoid cycle in cones (daylight vision) pathway
Retinoid cycle disease events pathway
Signaling by GPCR pathway
Signal Transduction pathway
GPCR downstream signaling pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
GPCR ligand binding pathway
Disease pathway
Signaling by GPCR pathway
Opsins pathway
Visual phototransduction pathway
G alpha (i) signalling events pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
GPCR downstream signaling pathway
GPCR ligand binding pathway
Class A/1 (Rhodopsin-like receptors) pathway
Retinoid cycle disease events pathway
Disease pathway
The retinoid cycle in cones (daylight vision) pathway
|
||||||||
| KEGG | |||||||||
| INOH | |||||||||
| PID NCI | |||||||||
| Cross-References | |||||||||
| SwissProt | |||||||||
| TrEMBL | |||||||||
| UniProt Splice Variant | |||||||||
| Entrez Gene | |||||||||
| UniGene | Mm.56987 | ||||||||
| RefSeq | NM_007538 XM_006504967 | ||||||||
| OMIM | |||||||||
| CCDS | CCDS19959 | ||||||||
| HPRD | |||||||||
| IMGT | |||||||||
| MGI ID | |||||||||
| MGI Symbol | |||||||||
| EMBL | |||||||||
| GenPept | |||||||||
| RNA Seq Atlas | |||||||||