centrosomal protein of 78 kDa isoform X3 [Rattus norvegicus]

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Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects. [Am J Hum Genet. 2016]
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.
Nikopoulos K, Farinelli P, Giangreco B, Tsika C, Royer-Bertrand B, Mbefo MK, Bedoni N, Kjellström U, El Zaoui I, Di Gioia SA, et al. Am J Hum Genet. 2016 Sep 1; 99(3):770-776.
Cep78 is a new centriolar protein involved in Plk4-induced centriole overduplication. [J Cell Sci. 2016]
Cep78 is a new centriolar protein involved in Plk4-induced centriole overduplication.
Brunk K, Zhu M, Bärenz F, Kratz AS, Haselmann-Weiss U, Antony C, Hoffmann I. J Cell Sci. 2016 Jul 15; 129(14):2713-8. Epub 2016 May 31.
The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis. [Biosci Rep. 2020]
The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis.
Li ZZ, Zhao WL, Wang GS, Gu NH, Sun F. Biosci Rep. 2020 Jan 31; 40(1).

RefSeq mRNA
See reference mRNA sequence for the Cep78 gene (XM_039088991.2).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the Cep78 gene.

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Protein