Homo sapiens SNF8 subunit of ESCRT-II (SNF8), transcript variant 3, mR - Nucleotide

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K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors. [Life Sci Alliance. 2024]
K48- and K63-linked ubiquitin chain interactome reveals branch- and length-specific ubiquitin interactors.
Waltho A, Popp O, Lenz C, Pluska L, Lambert M, Dötsch V, Mertins P, Sommer T. Life Sci Alliance. 2024 Aug; 7(8). Epub 2024 May 21.
Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy. [Am J Hum Genet. 2024]
Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy.
Brugger M, Lauri A, Zhen Y, Gramegna LL, Zott B, Sekulić N, Fasano G, Kopajtich R, Cordeddu V, Radio FC, et al. Am J Hum Genet. 2024 Mar 7; 111(3):594-613. Epub 2024 Feb 28.
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.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the SNF8 gene.
RefSeq protein product
See the reference protein sequence for vacuolar-sorting protein SNF8 isoform 3 (NP_001304122.1).

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Protein sequence from Nucleotide coding region
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Nucleotide