RD3 RD3 regulator of GUCY2D [ Homo sapiens (human) ]
Source: NCBI Gene (ID 343035)
Source: NCBI Gene (ID 343035)
Symbol: RD3
Full name: RD3 regulator of GUCY2D
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: C1orf36; LCA12
Summary: 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]
Expression: Low expression observed in reference dataset
Orthologs: mouse
Gene size: 15641bp
Exon count: 3