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RD3

Official Full Name
RD3 regulator of GUCY2D
Organism
Homo sapiens
GeneID
343035
Background
This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Synonyms
LCA12; C1orf36;

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