8iu2: Difference between revisions

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== Disease ==

[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] ~~Blue cone monochromatism;~~X-linked cone dysfunction syndrome with myopia;~~NON RARE IN EUROPE: Partial color blindness, protan type~~;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.

[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] X-linked cone dysfunction syndrome with myopia;Blue cone monochromatism;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.

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 </table>
 == Disease ==
-[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Blue cone monochromatism;X-linked cone dysfunction syndrome with myopia;NON RARE IN EUROPE: Partial color blindness, protan type;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
+[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] X-linked cone dysfunction syndrome with myopia;Blue cone monochromatism;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry.  The disease is caused by variants affecting the gene represented in this entry.
 == Function ==
 [https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.