coiled-coil domain-containing protein 66 isoform X4 [Rattus norvegicus - Protein

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Ccdc66 null mutation causes retinal degeneration and dysfunction. [Hum Mol Genet. 2011]
Ccdc66 null mutation causes retinal degeneration and dysfunction.
Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, et al. Hum Mol Genet. 2011 Sep 15; 20(18):3620-31. Epub 2011 Jun 16.
The centriolar satellite protein CCDC66 interacts with CEP290 and functions in cilium formation and trafficking. [J Cell Sci. 2017]
The centriolar satellite protein CCDC66 interacts with CEP290 and functions in cilium formation and trafficking.
Conkar D, Culfa E, Odabasi E, Rauniyar N, Yates JR 3rd, Firat-Karalar EN. J Cell Sci. 2017 Apr 15; 130(8):1450-1462. Epub 2017 Feb 24.
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene. [Neurogenetics. 2010]
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.
Dekomien G, Vollrath C, Petrasch-Parwez E, Boevé MH, Akkad DA, Gerding WM, Epplen JT. Neurogenetics. 2010 May; 11(2):163-74. Epub 2009 Sep 24.

RefSeq mRNA
See reference mRNA sequence for the Ccdc66 gene (XM_039095201.2).
RefSeq protein isoforms
See 17 reference sequence protein isoforms for the Ccdc66 gene.

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Protein