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OPN1MW information


OPN1MW
Identifiers
AliasesOPN1MW, CBBM, CBD, COD5, GCP, GOP, OPN1MW1, opsin 1 (cone pigments), medium-wave-sensitive, opsin 1, medium wave sensitive
External IDsOMIM: 300821 HomoloGene: 88332 GeneCards: OPN1MW
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000513

n/a

RefSeq (protein)

n/a

Location (UCSC)Chr X: 154.18 – 154.2 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Green-sensitive opsin is a protein that in humans is encoded by the OPN1MW gene.[3] OPN1MW2 is a similar opsin.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000268221 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Entrez Gene: OPN1MW opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)".

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OPN1MW

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Green-sensitive opsin is a protein that in humans is encoded by the OPN1MW gene. OPN1MW2 is a similar opsin. Opsin GRCh38: Ensembl release 89: ENSG00000268221...

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Cone cell

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S-cones, M-cones and L-cones. Each type expresses a different opsin: OPN1SW, OPN1MW, and OPN1LW, respectively. These cones are sensitive to visible wavelengths...

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OPN1LW

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while its counterparts, OPN1MW and OPN1SW, produce green-sensitive and blue-sensitive opsin respectively. OPN1LW and OPN1MW are on the X chromosome at...

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Tetrachromacy

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genes are present on the X chromosome: the classical type 2 opsin gene OPN1MW and OPN1MW2. People with two X chromosomes could possess multiple cone cell...

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Myopia

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PMID 23396134. Neitz M, Neitz J (August 2021). "Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders"...

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Color blindness

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deuteranopia/deuteranomaly. These conditions are mediated by the OPN1LW and OPN1MW genes, respectively, both on the X chromosome. An 'affected' gene is either...

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OPN1MW2

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OPN1MW2 is a duplication of the OPN1MW gene, which encodes the medium wavelength sensitive (MWS) photopsin. The gene duplication is present in about 50%...

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Color vision

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may therefore show a degree of tetrachromatic color vision. Variations in OPN1MW, which encodes the opsin expressed in M cones, appear to be rare, and the...

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Squirrel monkey

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that is most sensitive to the 564 nm wavelength, while the other gene (OPN1MW) produces a pigment most sensitive to 534 nm. In squirrel monkeys, there...

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Lysine

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opsins like rhodopsin and the visual opsins (encoded by the genes OPN1SW, OPN1MW, and OPN1LW), retinaldehyde forms a Schiff base with a conserved lysine...

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Retinal

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into the cytoplasm of the cell. The opsins in the cone cells are OPN1SW, OPN1MW, and OPN1LW. The cones form incomplete disks that are part of the plasma...

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Evolution of color vision in primates

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opsin genes on the X chromosome: M-opsin (middle wave sensitive, encoded by OPN1MW gene), the cone most sensitive to green light L-opsin (long wave sensitive...

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Achromatopsia

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achromatopsia. BCM stems from mutations or deletions of the OPN1LW and OPN1MW genes, both on the X chromosome. As a recessive x-linked condition, BCM...

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Vertebrate visual opsin

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variant Long-wave sensitive LWS Cone 500–570 OPN1LW "red" erythrolabe (564nm) OPN1MW "green" chlorolabe (534nm) Short-wave sensitive 1 SWS1 Cone 355–445 OPN1SW...

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Opsin

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3 photopsins in 2 classes: SWS1 (OPN1SW) and two forms of LWS (OPN1LW, OPN1MW). Scotopsins - those responsible for scotopic vision (dim light), which...

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Melanopsin

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regions, the pineal gland, and the skin. Paralogs of Opn4 include OPN1LW, OPN1MW, rhodopsin and encephalopsin. Melanopsin, like all other animal opsins (e...

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Locus control region

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(OPSIN-LCR) controlling the expression of OPN1LW and the first copies of OPN1MW on the human X chromosome, upstream of these genes. A dysfunctional LCR...

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List of OMIM disorder codes

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111150; KLF1 Bloom syndrome; 210900; RECQL3 Blue cone monochromacy; 303700; OPN1MW Blue cone monochromacy; 303700; OPN1LW Boomerang dysplasia; 112310; FLNB...

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