Nucleoporin 43

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Nucleoporin 43 (Nup43) is a protein that in humans is encoded by the NUP43 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesNUP43, bA350J20.1, p42, nucleoporin 43kDa, nucleoporin 43
Quick facts NUP43, Available structures ...
NUP43
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNUP43, bA350J20.1, p42, nucleoporin 43kDa, nucleoporin 43
External IDsOMIM: 608141; MGI: 1917162; HomoloGene: 11639; GeneCards: NUP43; OMA:NUP43 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024647
NM_198887

NM_145706

RefSeq (protein)

NP_942590

NP_663752

Location (UCSC)Chr 6: 149.72 – 149.75 MbChr 10: 7.54 – 7.55 Mb
PubMed search[3][4]
Wikidata
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Bidirectional transport of macromolecules between the cytoplasm and nucleus occurs through nuclear pore complexes (NPCs) embedded in the nuclear envelope. NPCs are composed of subcomplexes, and NUP43 is part of one such subcomplex, Nup107-160 (Loiodice et al., 2004).[supplied by OMIM][6] Along with other nucleoporins.

Structure

It folds into a canonical WD40 repeat domain.[7][8]

Disease association

High expression of NUP43 in breast cancer is associated with poor overall survival.[9] In chronic myelogenous leukemia (CML), reduction of miRNA-409-5p increases the expression of NUP43 that in turn enhances proliferative potential, cell cycle progression, and imatinib resistance.[10]

Some Nup43 variants have been characterized as causal for the onset of cardiovascular disease (CVD),[11] while Nup43 expression has been associated with attention deficit hyperactivity disorder.[12]

References

Further reading

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