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Summary Expression Phenotypes Gene Literature (0) GO Terms (0) Nucleotides (57) Proteins (37) Interactants (5) Wiki

pitpnm3     PITPNM family member 3

Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (9 sources): Abnormality of retinal pigmentation, Color vision defect, Cone dystrophy, Cone/cone-rod dystrophy, Macular degeneration, Nyctalopia, Photophobia, Reduced visual acuity, Visual impairment

View all ortholog results at Monarch