OPN1MW

GENERAL INFORMATION

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Gene name

OPN1MW

Gene description

Opsin 1 (cone pigments), medium-wave-sensitive

Protein class

Disease related genes
G-protein coupled receptors
Potential drug targets
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Not detected

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Not detected

Organ

Expression



GENE INFORMATION

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Gene name

OPN1MW (HGNC Symbol)

Synonyms

CBBM, CBD, COD5, GCP, OPN1MW1

Description

Opsin 1 (cone pigments), medium-wave-sensitive (HGNC Symbol)

Entrez gene summary

This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009]

Chromosome

X

Cytoband

q28

Chromosome location (bp)

154182596 - 154196135

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000268221 (version 78.38)

Entrez gene

2652

UniProt

P04001 (UniProt - Evidence at protein level)

neXtProt

NX_P04001

Antibodypedia

OPN1MW antibodies


PROTEIN BROWSER

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ENST00000595290
 
ENST00000596998
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

OPN1MW-001 ENSP00000472316
ENST00000595290
P04001
Show all »
Show » Show » 364 40.6 No 7
OPN1MW-002 ENSP00000469055
ENST00000596998
Show » Show » 164 18.1 No 2