Red Color Blindness malady

MalaCards: Red Color Blindness, also known as protan defect (disorder), is related to blindness and color blindness. An important gene associated with Red Color Blindness is ISX (intestine-specific homeobox). Related mouse phenotype no phenotypic analysis.

Aliases & Descriptions:

red color blindness 6 8 protan defect (disorder) 6 color blindness, red 43

protan defect 6 protanopia 6

Diseases related to red color blindness by text searches and GeneDecks gene sharing:

id	Related Disease	Score	Top Affiliating Genes
1	blindness	12.1	ISX, RORC
2	color blindness	11.8	ISX, RORC
3	red-green color blindness	9.1

Approved drugs:

Drug clinical trials:

MGI Mouse Phenotypes related to red color blindness:

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id	Description	MGI Source Accession	Score	Top Affiliating Genes
1	no phenotypic analysis	MP:0003012	9.1	ISX, RORC

Genes related to red color blindness according to GeneCards:

id	Symbol	Description	Score	GeneCards Section Context
1	ISX	intestine-specific homeobox	11.0
2	RORC	RAR-related orphan receptor C	11.0

Molecular functions related to red color blindness according to GeneDecks:

id	Name	GO ID	Score	Top Affiliating Genes
1	sequence-specific DNA binding	GO:043565	9.1	ISX, RORC