Homo sapiens nucleoporin 93 (NUP93), transcript variant 3, mRNA

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Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children. [Ital J Pediatr. 2024]
Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children.
Han Y, Sha H, Yang Y, Yu Z, Zhou L, Wang Y, Yang F, Qiu L, Zhang Y, Zhou J. Ital J Pediatr. 2024 Apr 22; 50(1):81. Epub 2024 Apr 22.
Nucleoporin93 limits Yap activity to prevent endothelial cell senescence. [Aging Cell. 2024]
Nucleoporin93 limits Yap activity to prevent endothelial cell senescence.
Nguyen TD, Rao MK, Dhyani SP, Banks JM, Winek MA, Michalkiewicz J, Lee MY. Aging Cell. 2024 Apr; 23(4):e14095. Epub 2024 Feb 13.
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.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the NUP93 gene.
RefSeq protein product
See the reference protein sequence for nuclear pore complex protein Nup93 isoform 2 (NP_001229725.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Functional Class
Functional class of the sequence domain architecture
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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SNP
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