Homo sapiens exosome component 8 (EXOSC8), RefSeqGene on chromosome 13

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Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
A missense variant in EXOSC8 causes exon skipping and expands the phenotypic spectrum of pontocerebellar hypoplasia type 1C. [J Hum Genet. 2024]
A missense variant in EXOSC8 causes exon skipping and expands the phenotypic spectrum of pontocerebellar hypoplasia type 1C.
Zaki MS, Abdel-Ghafar SF, Abdel-Hamid MS. J Hum Genet. 2024 Feb; 69(2):79-84. Epub 2023 Nov 29.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens exosome component 8 (EXOSC8), RefSeqGene on chromosome 13
Homo sapiens exosome component 8 (EXOSC8), RefSeqGene on chromosome 13
gi|908212445|ref|NG_042275.1|

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Nucleotide