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OPN1LW

OPN1LW

Protein-coding gene in humans.

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Wikipedia views per dayLast 30 days 352

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Share of the 85 clicks on its links

  1. Color blindness

    Decreased ability to see color or color differences.

    41%

  2. Opsin

    Class of light-sensitive proteins.

    31%

  3. OPN1MW

    Protein-coding gene in the species Homo sapiens.

    28%

Readers come from

Share of the 654 readers arriving from another article

  1. Cone cell

    Photoreceptor cells responsible for color vision made to function in bright light.

    24%

  2. Tetrachromacy

    Type of color vision with four types of cone cells.

    19%

  3. Opsin

    Class of light-sensitive proteins.

    17%

  4. Color blindness

    Decreased ability to see color or color differences.

    14%

  5. Vertebrate visual opsin

    Vision proteins.

    10%

  6. Congenital red–green color blindness

    Most common genetic condition leading to color blindness.

    9%

  7. OPN1SW

    Protein-coding gene in the species Homo sapiens.

    3.5%

  8. Cat senses

    Senses of Felis catus.

    2.1%

  9. OPN1MW

    Protein-coding gene in the species Homo sapiens.

    1.5%