centrosomal protein of 85 kDa-like isoform X5 [Homo sapiens]

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Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature. [Am J Med Genet A. 2023]
Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature.
Leduc-Pessah H, White-Brown A, Miller E, McMillan HJ, Boycott KM. Am J Med Genet A. 2023 Dec; 191(12):2878-2883. Epub 2023 Aug 25.
Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly. [Neuron. 2020]
Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly.
Tsai MH, Muir AM, Wang WJ, Kang YN, Yang KC, Chao NH, Wu MF, Chang YC, Porter BE, Jansen LA, et al. Neuron. 2020 Apr 22; 106(2):237-245.e8. Epub 2020 Feb 24.
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defects. [Neuropediatrics. 2003]
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defects.
Deconinck N, Duprez T, des Portes V, Beldjord C, Ghariani S, Sindic CJ, Sébire G. Neuropediatrics. 2003 Jun; 34(3):146-8.

RefSeq genomic sequence
See the genomic reference sequence for the CEP85L gene (NG_021248.1).
RefSeq mRNA
See reference mRNA sequence for the CEP85L gene (XM_054355404.1).
RefSeq protein isoforms
See 26 reference sequence protein isoforms for the CEP85L gene.

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Protein