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NUP85

Gene

nucleoporin 85

HGNCHGNC:8734EnsemblENSG00000125450NCBI Gene79902
Locus: gene with protein productLocation: 17q25.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asNUP75 · FLJ12549
View full nomenclature history (3)
Alias symbolsNUP75, FLJ12549
Previous namesnucleoporin 85kDa

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Nephrotic Syndrome
HIV Infections
Influenza, Human
Virus Diseases
Microcephalic primordial dwarfism
Seckel syndrome
COVID-19
Scleroderma, Systemic

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Nucleoporins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.