Symbol:
Opn1mw
Name:
opsin 1, medium wave sensitive
RGD ID:
620978
Description:
Predicted to enable G protein-coupled photoreceptor activity and identical protein binding activity. Predicted to be involved in several processes, including cellular response to light stimulus; phototransduction; and positive regulation of cytokinesis. Located in photoreceptor outer segment. Human ortholog(s) of this gene implicated in blue cone monochromacy; red color blindness; and red-green color blindness. Orthologous to several human genes including OPN1LW (opsin 1, long wave sensitive) and OPN1MW (opsin 1, medium wave sensitive); PARTICIPATES IN retinoid cycle metabolic pathway; visual phototransduction pathway; INTERACTS WITH 17alpha-ethynylestradiol; ammonium chloride; bisphenol A.
Type:
protein-coding
RefSeq Status:
VALIDATED
Previously known as:
green cone photoreceptor pigment; green-sensitive opsin; medium wavelength-sensitive cone opsin; medium-wave-sensitive opsin 1; opsin 1 (cone pigments), medium-wave-sensitive; opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan); opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan), green opsin
RGD Orthologs
Alliance Genes
More Info
more info ...
More Info
Species
Gene symbol and name
Data Source
Assertion derived from
less info ...
Orthologs 1
Homo sapiens (human):
OPN1MW (opsin 1, medium wave sensitive)
HGNC
Ensembl, Inparanoid, OMA, OrthoDB, Panther
Mus musculus (house mouse):
Opn1mw (opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan))
Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Sus scrofa (pig):
LOC494564 (medium-wave-sensitive opsin)
Transitive Ortholog Pipeline
Transitive Ortholog Pipeline
Other homologs 2
Homo sapiens (human):
OPN1LW (opsin 1, long wave sensitive)
HGNC
Ensembl, HomoloGene, OMA, Panther
Homo sapiens (human):
OPN1MW2 (opsin 1, medium wave sensitive 2)
HGNC
Ensembl, OMA, OrthoDB, Panther
Homo sapiens (human):
OPN1MW3 (opsin 1, medium wave sensitive 3)
HGNC
Ensembl, OMA, OrthoDB, Panther
Alliance orthologs 3
Mus musculus (house mouse):
Opn1mw (opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan))
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoFinder|OrthoInspector|PANTHER|PhylomeDB|SonicParanoid)
Homo sapiens (human):
OPN1LW (opsin 1, long wave sensitive)
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoFinder|OrthoInspector|PANTHER|PhylomeDB|SonicParanoid)
Homo sapiens (human):
OPN1MW (opsin 1, medium wave sensitive)
Alliance
DIOPT (Ensembl Compara|HGNC|Hieranoid|InParanoid|OMA|OrthoFinder|OrthoInspector|PANTHER|SonicParanoid)
Homo sapiens (human):
OPN1MW2 (opsin 1, medium wave sensitive 2)
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoFinder|OrthoInspector|PANTHER|SonicParanoid)
Homo sapiens (human):
OPN1MW3 (opsin 1, medium wave sensitive 3)
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoFinder|OrthoInspector|PANTHER|SonicParanoid)
Danio rerio (zebrafish):
opn1lw2 (opsin 1 (cone pigments), long-wave-sensitive, 2)
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoInspector|PANTHER|PhylomeDB|SonicParanoid)
Danio rerio (zebrafish):
opn1lw1 (opsin 1 (cone pigments), long-wave-sensitive, 1)
Alliance
DIOPT (Ensembl Compara|Hieranoid|InParanoid|OMA|OrthoInspector|PANTHER|PhylomeDB|SonicParanoid)
Latest Assembly:
mRatBN7.2 - mRatBN7.2 Assembly
Position:
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl mRatBN7.2 X 151,905,096 - 151,925,322 (+) NCBI mRatBN7.2 mRatBN7.2 mRatBN7.2 Ensembl X 151,905,096 - 151,925,388 (+) Ensembl mRatBN7.2 Ensembl UTH_Rnor_SHR_Utx X 154,046,219 - 154,066,443 (+) NCBI Rnor_SHR UTH_Rnor_SHRSP_BbbUtx_1.0 X 157,609,455 - 157,629,679 (+) NCBI Rnor_SHRSP UTH_Rnor_WKY_Bbb_1.0 X 155,281,257 - 155,301,483 (+) NCBI Rnor_WKY Rnor_6.0 X 156,569,683 - 156,589,907 (-) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_6.0 Ensembl X 156,569,683 - 156,589,907 (-) Ensembl Rnor6.0 rn6 Rnor6.0 Rnor_5.0 1 152,310,261 - 152,330,485 (-) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 X 160,095,742 - 160,115,966 (+) NCBI RGSC3.4 RGSC_v3.4 rn4 RGSC3.4 RGSC_v3.1 X 160,171,359 - 160,191,584 (+) NCBI Celera 1 135,969,802 - 135,990,029 (-) NCBI Celera Cytogenetic Map X q37 NCBI
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Imported Disease Annotations - ClinVar