Homo sapiens NADH:ubiquinone oxidoreductase complex assembly factor 8 - Nucleotide

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Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency. [Am J Hum Genet. 2020]
Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency.
Alston CL, Veling MT, Heidler J, Taylor LS, Alaimo JT, Sung AY, He L, Hopton S, Broomfield A, Pavaine J, et al. Am J Hum Genet. 2020 Jan 2; 106(1):92-101. Epub 2019 Dec 19.
Architecture of the human interactome defines protein communities and disease networks. [Nature. 2017]
Architecture of the human interactome defines protein communities and disease networks.
Huttlin EL, Bruckner RJ, Paulo JA, Cannon JR, Ting L, Baltier K, Colby G, Gebreab F, Gygi MP, Parzen H, et al. Nature. 2017 May 25; 545(7655):505-509. Epub 2017 May 17.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the NDUFAF8 gene.
RefSeq protein product
See the reference protein sequence for NADH dehydrogenase (NP_001340332.1).

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Nucleotide