PREDICTED: Homo sapiens centrosomal protein 164 (CEP164), transcript v - Nucleotide

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Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome. [Clin Genet. 2023]
Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome.
Devlin LA, Coles J, Jackson CL, Barroso-Gil M, Green B, Walker WT, Thomas NS, Thompson J, Rock SA, Neatu R, et al. Clin Genet. 2023 Mar; 103(3):330-334. Epub 2022 Nov 3.
OpenCell: Endogenous tagging for the cartography of human cellular organization. [Science. 2022]
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Cho NH, Cheveralls KC, Brunner AD, Kim K, Michaelis AC, Raghavan P, Kobayashi H, Savy L, Li JY, Canaj H, et al. Science. 2022 Mar 11; 375(6585):eabi6983. Epub 2022 Mar 11.
Molecular mechanisms underlying the role of the centriolar CEP164-TTBK2 complex in ciliopathies. [Structure. 2022]
Molecular mechanisms underlying the role of the centriolar CEP164-TTBK2 complex in ciliopathies.
Rosa E Silva I, Binó L, Johnson CM, Rutherford TJ, Neuhaus D, Andreeva A, Čajánek L, van Breugel M. Structure. 2022 Jan 6; 30(1):114-128.e9. Epub 2021 Sep 8.

RefSeq protein product
See the reference protein sequence for centrosomal protein of 164 kDa isoform X9 (XP_054224035.1).

PREDICTED: Homo sapiens centrosomal protein 164 (CEP164), transcript variant X10...
PREDICTED: Homo sapiens centrosomal protein 164 (CEP164), transcript variant X10, mRNA
gi|2462523731|ref|XM_054368060.1|

Nucleotide
LOC127268632 [Homo sapiens]
LOC127268632 [Homo sapiens]
Gene ID:127268632

Gene

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Nucleotide